Process for producing hydroxyarenes

Details Process for producing hydroxyarenes Process for producing hydroxyarenes

1998-11-12

2001-01-09

McKane, Joseph (Department: 1613)

Organic compounds -- part of the class 532-570 series

Organic compounds

Nitrogen attached directly or indirectly to the purine ring...

C548S263200, C548S377100, C548S366100, C558S425000

Reexamination Certificate

active

06172225

ABSTRACT:

TECHNICAL FIELD OF THE INVENTION
The invention relates to a novel process for producing thereof hydroxyarenes which can be used as active compounds or as intermediates for preparing active compounds, in particular herbicides.
BACKGROUND OF THE INVENTION
Methods for the preparation of hydroxyarenes (“phenols”) have been known for a long time and are part of the “textbook knowledge” of organic chemistry. Hydroxyarenes are generally prepared by reaction of metal hydroxides with arenes containing groups which are easily nucleophilically substitutable. With this approach, problems may occur if the starting materials contain other groups which are easily attacked by a nucleophilic mechanism, such as, for example, cyano or ester groups. Undesirable side reactions are also observed in the alternatively possible synthesis by cleavage of appropriate methoxyarenes (cf. DE-A 38 35 168 and Bull. Korean Chem. Soc. 14 (1993), 717). It is an object of the present invention to provide a process which makes it possible to introduce hydroxy groups into arenes without affecting other groups which are easily attacked, such as, in particular, the cyano group.
DETAILED DESCRIPTION OF THE INVENTION
This invention, accordingly, provides hydroxyarenes of the general formula (I)
in which
n represents the numbers 1, 2, 3 or 4,
R represents cyano, carboxyl, formyl, nitro, halogen or represents alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylcarbonyl or alkoxycarbonyl, each of which is optionally substituted, and
z represents hydrogen, cyano, nitro, halogen, alkyl, halogenoalklyl, or represents monocyclic or bicyclic, saturated or unsaturated heterocyclyl, heterocyclylamino or heterocyclylimino, each of which is optionally substituted,
in high yields and in good quality
by reaction of halogenoarenes of the general formula (II)
in which
n, R and Z are each as defined above and
X represents halogen
with 3-hydroxy-propionitrile of the formula (III)
HO—CH
2
CH
2
—CN  (III),
if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, at temperatures between 0° C. and 100° C.
Surprisingly, it is possible using the process according to the invention to obtain hydroxyarenes of the general formula (I) in a simple and gentle manner in high yields and in good quality without affecting groups, such as, in particular, cyano groups, which are sensitive towards nucleophiles.
The process according to the invention therefore represents a useful addition to the prior art.
The process according to the invention preferably relates to the preparation of compounds of the formula (I) in which
n represents the numbers 1, 2 or 3,
R represents cyano, carboxyl, formyl, nitro, halogen or represents alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylcarbonyl or alkoxycarbonyl having in each case 1 to 6 carbon atoms and being in each case optionally substituted by cyano, halogen, C
1
-C
4
-alkoxy or C
1
-C
4
-alkylthio,
Z represents hydrogen, cyano, halogen or represents monocyclic or bicyclic, saturated or unsaturated heterocyclyl, heterocyclylamino or heterocyclylimino having in each case 2 to 6 carbon atoms and 1 to 4 nitrogen atoms in the heterocyclic ring system and being in each case optionally substituted, which optionally additionally contains an oxygen or sulphur atom and or optionally up to three groups selected from the series —CO—, —CS—, —SO— and/or SO
2
—, and which is optionally substituted by one or more groups selected from the series nitro, hydroxyl, amino, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, C
1
-C
6
-alkyl (which is optionally substituted by halogen or C
1
-C
4
-alkoxy), C
2
-C
6
-alkenyl or C
2
-C
6
-alkinyl (which are in each case optionally substituted by halogen), C
1
-C
6
-alkoxy or C
1
-C
6
-alkoxy-carbonyl (which are in each case optionally substituted by halogen or C
1
-C
6
-alkoxy), C
2
-C
6
-alkenyloxy or C
2
-C
6
-alkinyloxy (which are in each case optionally substituted by halogen), C
1
-C
6
-alkylthio, C
2
-C
6
-alkenylthio or C
2
-C
6
-alkinylthio (which are in each case optionally substituted by halogen), C
1
-C
6
-alkylamino or di-(C
1
-C
4
-alkyl)-amino, C
3
-C
6
-cycloalkyl or C
3
-C
6
-cycloalkyl-C
1
-C
4
-alkyl (which are in each case optionally substituted by halogen and/or C
1
-C
4
-alkyl), phenyl, phenoxy, phenylthio, phenylsulphinyl, phenylsulphonyl or phenylamino (which are in each case optionally substituted by nitro, cyano, halogen, C
1
-C
4
-alkyl, C
1
-C
4
-halogenoalkyl, C
1
-C
4
-alkyloxy, C
1
-C
4
-halogenoalkyloxy and/or C
1
-C
4
-alkoxy-carbonyl).
The process according to the invention in particular relates to the preparation of compounds of the formula (I) in which
n represents the numbers 1 or 2,
R represents cyano, carboxyl, formyl, nitro, halogen or represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl, ethylsulphonyl, acetyl, propionyl, methoxycarbonyl or ethoxycarbonyl, each of which is optionally substituted by cyano, halogen, methoxy, ethoxy, methylthio or ethylthio,
Z represents hydrogen, cyano, halogen or represents monocyclic or bicyclic, saturated or unsaturated heterocyclyl, heterocyclylamino or heterocyclylimino having in each case 2 to 6 carbon atoms and 1 to 4nitrogen atoms in the heterocyclic ring system and being in each case optionally substituted, which optionally additionally contains an oxygen or sulphur atom and/or optionally up to two groups selected from the series —CO—, —CS—, —SO— and/or SO
2
—, and which is optionally substituted by one or more groups selected from the series nitro, hydroxyl, amino, cyano, carboxyl, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine; methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl (which are optionally substituted by fluorine, chlorine, methoxy or ethoxy); propenyl, butenyl, propinyl or butinyl (which are in each case optionally substituted by fluorine or chlorine); methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methoxycarbonyl or ethoxycarbonyl (which are in each case optionally substituted by fluorine, chlorine, methoxy or ethoxy); propenyloxy, butenyloxy, propinyloxy or butinyloxy (which are optionally substituted by fluorine or chlorine); methylthio, ethylthio, n- or i-propylthio, n-, i-. s- or t-butylthio, propenylthio, butenylthio, propinylthio or butinylthio (which are in each case optionally substituted by fluorine or chlorine); methylamino, ethylamino, n- or i-propylamino, n-, i-. s- or t-butylamino, dimethylamino or diethylamino; cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl (which are in each case optionally substituted by fluorine, chlorine, methyl, ethyl n- or i-propyl), phenyl, phenoxy, phenylthio, phenylsulphinyl, phenylsulphonyl or phenylamino (which are in each case optionally substituted by nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, trifluoromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy, trifluoromethoxy, methoxycarbonyl or ethoxycarbonyl).
Z in the formulae (I) and (II) represents in particular the heterocyclic groups listed below:
where in each case
Q
1
represents a group selected from the series —CO—, —CS—, —CH
2
—, —CH(OH)—, —CHCl—, —CHBr—, —C(═CH
2
)—, —C(═CHF)—, —C(═CF
2
)—, —C(═CHCl)—, —C(═CHBr)—, —C(═CHOCHF
2
)—, —C(═CHOCF
3
)—, —C(═CHOCH
2
CF
3
)—,
Q
2
represents oxygen, sulphur or a group selected from the series —CO—, —CS—, —CH
2
—, —CHF—, —CF
2
—, —CHCl—, CHBr—, —CHOCHF
2
—, —CHOCF
3
—, —CHOCH
2
CF
3
—,
A
1
represents hydrogen, amino, nitro, cyano, carboxyl, carbamoyl, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, cyclopropyl, difluoromethyl, trifluoromethyl, chlorodifluoromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, trifluoromethylthio, chlorodifluor

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