Method for preparing silicon with high purity ester function

Details Method for preparing silicon with high purity ester function Method for preparing silicon with high purity ester function

2000-08-15

2002-09-24

Dawson, Robert (Department: 1712)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Mixing of two or more solid polymers; mixing of solid...

C525S474000, C528S031000, C528S029000, C528S026000, C528S501000, C528S490000, C556S437000

Reexamination Certificate

active

06455641

ABSTRACT:

This application is an application under 35 U.S.C. Section 371 of International Application Number PCT/FR98/02897 filed on Dec. 29, 1998.
The present invention relates to a method for preparing polyorganosiloxanes (silicones) with an ester function (acetoxyalkyl or acetoxyalkenyl) of high purity, primarily free of functions or by-products with an &agr;-olefinic unsaturated bond.
The invention provides a method for producing polyorganosiloxanes with ester functions with formula (I):
R
1
R
2
R
3
SiO(R
4
R
5
SiO)
p
(R
6
QSiO)
q
SiR
3
R
2
R
1
  (I),
where:
symbols R
1
, R
2
are identical or different and represent:
a C
1
to C
6
alkyl radical or a phenyl radical, preferably methyl;
or a —OR
7
radical, where R
7
represents a linear or branched C
1
to C
6
alkyl radical, preferably methyl;
symbols R
4
, R
5
and R
6
are identical or different and represent a C
1
to C
6
alkyl radical or a phenyl radical, preferably methyl;
symbols R
3
, which may be identical or different, represent:
a linear or branched C
1
to C
6
alkyl radical or a phenyl radical, preferably methyl;
the symbol Q;
or a —OR
7
group, where R
7
represents a linear or branched C
1
to C
6
alkyl radical, preferably methyl;
symbols Q, which may be identical or different, represent an ester function or an alcohol function, respectively with formulae (1) and (2) below:
—R′OCOR″  (1)
—R′OH  (2)
where:
R′ represents a linear or branched C
3
-C
20
alkylene group, preferably C
3
-C
12
, more particularly trimethylene or 2-methyltrimethylene;
R″ represents a methyl group;
at least one of symbols Q representing an ester function with formula (1);
p represents an average number of 0 or more, preferably more than 5;
q represents an average number of 0 or more, preferably more than 1; at least one of symbols R
3
representing the ester symbol Q of formula (1) when q equals 0;
by hydrosilylation between a hydrogeno-polyorganosiloxane with formula II):
R
1
R
2
R
3
SiO(R
4
R
5
SiO)
p
(R
6
HSiO)
q
SiR
3
R
2
R
1
  (II)
where:
symbols R
1
, R
2
, R
4
, R
5
, R
6
, p and q have the definitions given above;
symbols R
3
′, which may be identical or different, represent:
a linear or branched C
1
to C
6
alkyl radical or a phenyl radical, preferably methyl;
H;
or a —OR
7
group, where R
7
represents a linear or branched C, to C
6
alkyl radical, preferably methyl;
and an &agr;-olefinic alcohol with formula ROH, where R represents an &agr;-olefinic radical from which the divalent radical R′ derives by opening of the &agr; double bond and adding hydrogen, preferably an allyl or methallyl radical;
then esterification of the hydroxy-alkylated polyorganosiloxane with formula (III) obtained:
R
1
R
2
R
3″
SiO(R
4
R
5
SiO)
p
(R
6
Q′SiO)
q
SiR
3″
R
2
R
1
  (III)
where:
symbols R
1
, R
2
, R
4
, R
5
, R
6
, p and q have the definitions given above;
symbols R
3
″, which may be identical or different, represent:
a linear or branched C
1
to C
6
alkyl radical or a phenyl radical, preferably methyl;
the symbol Q′;
or a —OR
7
group, where R
7
has the definition given above;
symbol Q′ represents the radical R′OH, where R′ has the definition given above; with an acyl halide with formula XCOR″, where X represents a halogen atom, in particular chlorine, and R″ has the definition given above, in the absence of an esterification catalyst;
and eliminating the &agr; olefinic by-products and the hydrohalic acid formed.
The hydrosilylation step can be carried out in any known manner at a temperature of the order of 20° C. to 200° C., preferably of the order of 60° C. to 120° C., in the presence of a hydrosilylation catalyst. Examples which can be cited are those based on platinum such as the platinum complexes described in U.S. Pat. No. 3,159,601, U.S. Pat. No. 3,159,662, U.S. Pat. No. 3,715,334, U.S. Pat. No. 3 ,14,730. A conventional catalyst is the KARSTEDT catalyst used, for example, in an amount of 1 to 300 parts, preferably 5 to 50 parts, by weight of platinum per million parts by weight of reactants.
The relative quantities of hydrogeno-polyorganosiloxane with formula (II) and &agr;-olefinic alcohol ROH generally correspond to an &agr;-olefinic alcohol/hydrogeno-polyorganosiloxane mole ratio more than 1 and less than or equal to 5, preferably more than 1 and less than or equal to 2.
In defining the moles of (&agr;-olefinic alcohol, the elementary entity is considered to be the &agr;-olefinic unsaturated bond; in defining the moles of hydrogeno-polyorganosiloxane, the elementary entity is considered to be the SiH function.
The hydrosilylation operation can be carried out at atmospheric pressure, preferably in bulk; however, it can be carried out in an organic solvent such as toluene, xylene, methylcycyclohexane, heptane, octane, hexamethylsiloxane.
The operation is carried out until the —SiH groups in the reaction mass have disappeared. The operation can be monitored by infrared analysis or volumetric determination.
The excess &agr;-olefinic alcohol can be eliminated by vacuum distillation (for example 13 Pa to 14000 Pa).
The hydrogeno-polyorganosiloxane used in the hydrosilylation step is preferably selected from those with formulae:
Me
3
SiO(SiMe
2
O)
p′
(SiMeHO)
q′
SiMe
3
Me
2
HSiO(SiMe
2
O)
p′
(SiMeHO)
q′
SiHMe
2
Me
2
HSiO(SiMe
2
O)
p″
SiHMe
2
where:
Me represents the methyl radical;
p′ represents an average number of the order of 0 to 500, preferably of the order of 5 to 100;
p″ represents an average number of the order of 0 to 100, preferably of the order of 0 to 20;
q′ represents an average number of the order of 1 to 50, preferably of the order of 1 to 30.
The &agr;-olefinic alcohol with formula ROH used in the hydrosilylation step is preferably allyl alcohol or methallyl alcohol.
The esterification operation can be carried out at a temperature of the order of 0° C. to 100° C., preferably of the order of 15° C. to 50° C., more particularly of the order of 15° C. to 30° C.
The relative quantities of hydroxyalkylated polyorganosiloxane and acyl halide with formula XCOR″ generally correspond to an acyl halide/hydroxyalkylated polyorganosiloxane mole ratio of the order of 0.1 to 2, preferably of the order of 0.1 to 1.
In defining the moles of hydroxyalkylated polyorganosiloxane, the elementary entity is considered to be the hydroxyalkyl function.
The esterification operation can be carried out at atmospheric pressure, preferably in bulk; however, it can be carried out in an organic solvent such as toluene, xylene, methylcyclohexane, heptane, octane, hexamethylsiloxane.
The acyl halide with formula XCOR″ used in the esterification step is preferably acetyl chloride.
The acid halide formed by esterification can be eliminated by entraining it in an inert gas (argon, nitrogen . . . ) then by treatment with a base, such as alkali metal bicarbonates, in particular sodium bicarbonate, in stoichiometric excess over the acyl halide (for example 2 to 3 times the stoichiometry).
After eliminating the by-products by condensing under reduced pressure, the polyorganosiloxane with an ester function can then be recovered by filtering, for example.
&agr;-olefinic siloxane motifs and &agr;-olefinic impurities are those with formulae ═Si—O—R, ROH and R″COOR, where R represents a linear or branched &agr;-olefinic radical containing 3 to 20 carbon atoms, as defined above (allyl or methallyl, for example), and R″ is the methyl group.


REFERENCES:
patent: 3450736 (1969-06-01), Monterey
patent: 4725658 (1988-02-01), Thayer
patent: 0 336 141 (1989-10-01), None
patent: 0 446 938 (1991-09-01), None
patent: 0 523 738 (1993-01-01), None

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