Process for the preparation of bis(acyl)phospinic acid sylyl esters

Patent metadata

Field	Value
Publication number	US-10865219-B2
Application number	US-201816621163-A
Country	US
Kind code	B2
Filing date	Jun 27, 2018
Priority date	Jun 27, 2017
Publication date	Dec 15, 2020
Grant date	Dec 15, 2020

Abstract

The present invention refers to a process for the preparation of a bis(acyl)phosphinic acid silyl ester of the general formula (I), wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , R 10 and R 11 are the same or different and are independently selected from H, halogen, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl, C 1 -C 8 -alkoxy, C 2 -C 8 -alkenyloxy, C 3 -C 8 -cycloalkyl, C 6 -C 12 -aryl, C 3 -C 8 -cycloalkoxy, C 7 -C 12 -arylalkoxy, C 9 -C 15 -alkenylarylalkoxy, nitro-, C 6 -C 12 -arylsulfonyl, 4-alkylarylsulfonyl, C 1 -C 20 -alkylcarboxy, C 1 -C 8 -alkoxycarbonyl, SR 12 , NHR 12 or NR 12 R 13 with R 12 and R 13 being independently selected from H, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl and C 3 -C 8 -cycloalkyl, and an O-, S- or N-containing 5- or 6-membered heterocyclic ring; R 6 is OSiR 14 R 15 R 16 with R 14 , R 15 and R 16 being independently selected from linear or branched C 1 -C 20 -alkyl or C 6 -C 12 -aryl; as well as the bis(acyl)phosphinic acid silyl ester and the bis(acyl)phosphinic acid obtained by the process.

First claim

The invention claimed is:

1. A process for the preparation of a bis(acyl)phosphinic acid silyl ester of the general formula I:

wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , R 10 and R 11 are the same or different and are independently selected from H, halogen, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl, C 1 -C 8 -alkoxy, C 2 -C 8 -alkenyloxy, C 3 -C 8 -cycloalkyl, C 6 -C 12 -aryl, C 3 -C 8 -cycloalkoxy, C 7 -C 12 -arylalkoxy, C 9 -C 15 -alkenylarylalkoxy, nitro-, C 6 -C 12 -arylsulfonyl, 4-alkylarylsulfonyl, C 1 -C 20 -alkylcarboxy, C 1 -C 8 -alkoxycarbonyl, SR 12 , NHR 12 or NR 12 R 13 with R 12 and R 13 being independently selected from H, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl and C 3 -C 8 -cycloalkyl, and an O-, S- or N-containing 5- or 6-membered heterocyclic ring; R 6 is OSiR 14 R 15 R 16 with R 14 , R 15 and R 16 being independently selected from linear or branched C 1 -C 20 -alkyl or C 6 -C 12 -aryl,
the process comprising the steps of
a) heating ammonium hypophosphite with a silylating agent for obtaining a bis(silyl ether)phosphine, and
b) reacting the bis(silyl ether)phosphine obtained in step a) with a compound of the general formula IIa and/or IIb,

wherein R 1 , R 2 , R 3 , R 4 and R 5 and/or R 7 , R 8 , R 9 , R 10 and R 11 are as defined above; Z is halogen.

2. The process according to claim 1 , wherein R 1 , R 3 and R 5 and/or R 7 , R 9 and R 11 are the same.

3. The process according to claim 2 , wherein R 1 , R 3 and R 5 and/or R 7 , R 9 and R 11 are the same and are selected from linear or branched C 1 -C 20 -alkyl.

4. The process according to claim 1 , wherein R 2 and R 4 and/or R 8 and R 10 are the same.

5. The process according to claim 1 , wherein R 2 and R 4 and/or R 8 and R 10 are the same and are H.

6. The process according to claim 1 , wherein Z is selected from chloro, bromo and iodo.

7. The process according to claim 1 , wherein step a) is carried out under an inert gas atmosphere and/or without the addition of a solvent.

8. The process according to claim 1 , wherein the bis(silyl ether)phosphine obtained in step a) is mixed with an organic solvent before process step b) is carried out.

9. The process according to claim 1 , wherein the bis(silyl ether)phosphine obtained in step a) is subjected to process step b) without purification and isolation of the silylated product obtained in step a).

10. The process according to claim 1 , wherein step a) is carried out at a temperature in the range from 100 to 130° C. and/or step b) is carried out at a temperature in the range from −5 to 50° C.

11. The process according to claim 1 , wherein step b) is carried out in that the equivalent weight ratio of the compound of the general formula IIa and/or IIb to the ammonium hypophosphite of step a) [IIa and/or IIb:P-compound] is in the range from 3.5:1 to 1.5:1.

12. The process according to claim 1 , wherein process step a) and/or step b) is repeated one or more times.

13. The process according to claim 1 , wherein the process comprises a further step c) of hydrolyzing the bis(acyl)phosphinic acid silyl ester obtained in step b) such as to obtain a bis(acyl)phosphinic acid of the general formula III:

wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , R 10 and R 11 are the same or different and are independently selected from H, halogen, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl, C 1 -C 8 -alkoxy, C 2 -C 8 -alkenyloxy, C 3 -C 8 -cycloalkyl, C 6 -C 12 -aryl, C 3 -C 8 -cycloalkoxy, C 7 -C 12 -arylalkoxy, C 9 -C 15 -alkenylarylalkoxy, nitro-, C 6 -C 12 -arylsulfonyl, 4-alkylarylsulfonyl, C 1 -C 20 -alkylcarboxy, C 1 -C 8 -alkoxycarbonyl, SR 12 , NHR 12 or NR 12 R 13 with R 12 and R 13 being independently selected from H, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl and C 3 -C 8 -cycloalkyl, and an O-, S- or N-containing 5- or 6-membered heterocyclic ring; R 6 is OH.

14. The process according to claim 13 , wherein step c) is carried out at a temperature in the range from −5 to 50° C.

15. A bis(acyl)phosphinic acid silyl ester of the general formula I:

wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , R 10 and R 11 are the same or different and are independently selected from H, halogen, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl, C 1 -C 8 -alkoxy, C 2 -C 8 -alkenyloxy, C 3 -C 8 -cycloalkyl, C 6 -C 12 -aryl, C 3 -C 8 -cycloalkoxy, C 7 -C 12 -arylalkoxy, C 9 -C 15 -alkenylarylalkoxy, nitro-, C 6 -C 12 -arylsulfonyl, 4-alkylarylsulfonyl, C 1 -C 20 -alkylcarboxy, C 1 -C 8 -alkoxycarbonyl, SR 12 , NHR 12 or NR 12 R 13 with R 12 and R 13 being independently selected from H, linear or branched C 1 -C 20 -alkyl, linear or branched C 2 -C 8 -alkenyl and C 3 -C 8 -cycloalkyl, and an O-, S- or N-containing 5- or 6-membered heterocyclic ring; R 6 is OSiR 14 R 15 R 16 with R 14 , R 15 and R 16 being independently selected from linear or branched C 1 -C 20 -alkyl or C 6 -C 12 -aryl,
obtained by a process according to claim 1 .

Assignees

• Igm Group B V
• Borealis Ag

Inventors

• Sommerlade Reinhard H
• Luckner Kai Uwe

Classifications

• C07F9/3258

  the ester moiety containing a substituent or a structure which is considered as characteristic · CPC title

• C07F9/307 Primary

  Acids containing the structure -C(=X)-P(=X)(R)(XH) or NC-P(=X)(R)(XH), (X = O, S, Se) · CPC title

• C07F9/08

  Esters of oxyacids of phosphorus {(C07F9/062 takes precedence)} · CPC title

• C07F7/10

  containing nitrogen {having a Si-N linkage} · CPC title

• C07F9/5086 Primary

  from phosphonium salts as starting materials · CPC title