Process for preparing salts of dialkylphosphinic acids

Organic compounds -- part of the class 532-570 series – Organic compounds – Phosphorus acids or salts thereof

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

06534673

ABSTRACT:

The invention likewise relates to the use of the metal dialkylphosphinate salts prepared by the process according to the invention for preparing flame retardants.
Process for preparing salts of dialkylphosphinic acids
The invention relates to a process for preparing salts of dialkylphosphinic acids and to the use of the dialkylphosphinate salts prepared by this process.
Aluminum salts of organic phosphorus-containing acids are known as flame retardants. They can be prepared by various processes.
EP-A-0 299 922 describes a process for preparing aluminum salts of phosphoric and phosphonic esters by reacting aluminum with phosphoric acid, phosphonic acid or an ester thereof.
In the process described in EP-A-0 245 207, aluminum compounds are reacted with alkylphosphonic diesters to give the corresponding aluminum salt.
According to EP-A-0 327 496, the reaction of aluminum hydroxide with alkylphosphonic diesters in the absence of water at approximately 180° C. likewise leads to aluminum salts of phosphonic half-esters.
EP-A-0 699 708 describes flame-retardant polyester molding compounds, the polyesters being given a flameretardant finish by adding calcium salts or aluminum salts of phosphinic. or diphosphinic acids. The abovementioned salts are obtained by reacting the corresponding dialkylphosphinic acids with calcium hydroxide or aluminum hydroxide.
DE 24 47 727 describes low-flammability polyamide molding compounds which comprise a salt of a phosphinic acid or of a diphosphinic acid.
However, the abovementioned processes have the disadvantage that the suitable organic phosphorus compounds must first be prepared in a laborious manner. This applies, in particular, to the dialkylphosphinic acids, whose aluminum salts give the best results in the application as flame retardants, and for which, likewise, some synthetic pathways are described.
Thus DE 21 00 779 Al describes a process for preparing alkyl dialkylphosphinates by addition of olefins having from 2 to 22 carbon atoms to alkylphosphonous esters.
In this case also, there has been the lack to date of an economic synthesis method which leads to homogeneous products in a high yield.


REFERENCES:
patent: 2957931 (1960-10-01), Hamilton et al.
patent: 3488368 (1970-01-01), Spivack
patent: 3534127 (1970-10-01), Spivack
patent: 3563948 (1971-02-01), Spivack
patent: 3742096 (1973-06-01), Spivack
patent: 3912654 (1975-10-01), Heid et al.
patent: 3914345 (1975-10-01), Kleiner et al.
patent: 4036811 (1977-07-01), Noetzel
patent: 4208322 (1980-06-01), Sandler
patent: 4321187 (1982-03-01), Granzow
patent: 4590014 (1986-05-01), Wolf
patent: 4632741 (1986-12-01), Wolf et al.
patent: 4939285 (1990-07-01), Weis et al.
patent: 4972011 (1990-11-01), Richardson et al.
patent: 4973727 (1990-11-01), Gainer et al.
patent: 5780534 (1998-07-01), Kleiner et al.
patent: 6207736 (2001-03-01), Nass et al.
patent: 0327496 (1989-08-01), None
patent: 0699708 (1996-03-01), None
patent: 8505520 (1984-05-01), None
patent: 1 558 606 (1969-02-01), None
CA:10725119 abs of ES532346, Jun. 1985.*
CA:107:176590 abs of Bull. Chem Soc Jpn. by Ohno 60(8) pp. 2945-2951, 1987.*
E.E. Nifant'Ev: “Acid catalysis in the hydrophosphorylation of olefins” Journal of General Chemistry USSR., vol. 50, No. 8/1, -Aug. 1980, pp. 1416-1423, XP002093427, New York US.
E.E. Nifant'Ev: “Hydrophosphorylation of cyclopentenes” Journal of General Chemistry USSR., vol. 61, No. 1/1,-Jan. 1991 pp. 83-92, XP002093428 New York US.
Chemical Abstracts, vol. 69, No. 16, Oct. 14, 1968 Columbus, OH, US; abstract No. 067487, p. 6310 column 2; XP002093429 & Petrov K.A.: “Dialkylphosphinic acids”KHIM. ORG. SOEDIN. FOSFORA, AKAD. NAUK SSSR, OTD. OBSHCH. TEKH. KHIM., 1967, pp. 181-186, SU.
“Synthesis of DI(n-octyl)phosphinic acid. Influence of the sulfuric acide in the phosphination of 1-octene with sodium hypophosphite,” M. Martinez, C. Herranze, N. Miralles, & A. Sastre, AFINIDAD LIII, 466, 1996, pp. 404-406.
William C. Drinkard: “Some salts of symmetric phosphinic acids” Journal of the American Chemical Society., Bd. 74, Nr. 21, -5. Nov. 1952 Seiten 5520-5521, XP002093391.
Chemical abstracts vol. 64 abstrac No. 16661 g by Hoffman (6/66).
Houben-Weyl, Methoden der organischen Chemie, vol. XII/1, 4thEdition, 1963, p. 228ff.
“Phosphinsaure und dderen Derivate,” Dr. Felcht, vol. E2, 1982, p.123 ff.
CA:111:92772 abs of Arch Biochem Biophys by Morehouse et al., 273(1) pp. 158-64.
CA: 80:26559 abs of J Inorg Nucl Chem by Selbin., 35(10) pp. 3467-80.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Process for preparing salts of dialkylphosphinic acids does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Process for preparing salts of dialkylphosphinic acids, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for preparing salts of dialkylphosphinic acids will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3026773

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.