IP Library Patent Application 10504902
Patent Application
App. No. 10/504,902

Polyamino acids and method for producing the same

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Patent No.
US None
App. No.
10/504,902
Abstract

The invention relates to polyamino acids, to a method for producing the same and to their use as catalysts for enantioselective epoxidation of α,β-unsaturated enons and α,β-unsaturated sulfones.

Claims (20)

1 . A polyamino acid comprising reacting at least one amino acid-N-carboxy anhydrides with at least one initiator wherein the reacting of the at least one amino acid-N-carboxy anhydride and the at least one initiator is carried out under conditions in which

a) an aromatic solvent is used;

b) the reaction temperature is between 30° C. and the boiling point of the reaction mixture, and

c) the molar ratio of amino acid-NCA to the initiator is between 4:1 and 200:1.

2 . A method for producing polyamino acids comprising reacting amino acid-N-carboxy anhydrides with an initiator wherein the reacting of the at least one amino acid-N-carboxy anhydride and the at least one initiator is carried out under conditions in which

a) an aromatic solvent is used;

b) the reaction temperature is between 30° C. and the boiling point of the reaction mixture, and

c) the molar ratio of amino acid-NCA to the initiator is between 4:1 and 200:1.

3 . An process comprising converting a C—C double bond of compound into an oxirine, wherein the process is an epoxidation reaction carried out with a polyamino acid catalyst;

wherein the polyamino acid catalyst is made by a process involving reacting at least one amino acid-N-carboxy anhydride with at least one initiator

wherein the reacting of the at least one amino acid-N-carboxy anhydride and the at least one initiator is carried out under conditions in which

a) an aromatic solvent is used:

b) the reaction temperature is between 30° C. and the boiling point of the reaction mixture, and

c) the molar ratio of amino acid-NCA to the initiator is between 4:1 and 200:1.

4 . The process of claim 3 , wherein the C—C double bond is a C—C double bond of a compound selected from the group consisting of α,β-unsaturated enones, α,β-unsaturated sulfones.

5 . The process of claim 4 , wherein the ,β-unsaturated enones or α,β-unsaturated sulfones the compounds of the general formula (II)

in which

X is (C═O) or (SO 2 ), and

R 5 and R 6 are identical or different and are (C 1 -C 18 )-alkyl, (C 2 -C 18 )-alkenyl, (C 2 -C 18 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 6 -C 18 )-aryl, (C 7 -C 19 )-aralkyl, (C 1 -C 18 )heteroaryl or (C 2 -C 19 )-heteroaralkyl,

wherein the radicals mentioned for R 5 and R 6 may be substituted once or more than once by identical or different radicals R 7 , halogen, NO 2 , NR 7 R 8 , PO 0-3 R 7 R 8 , SO 0-3 R 7 , OR 7 , CO 2 R 7 , CONHR 7 or COR 7 , and optinoally one or more CH 2 groups in the radicals R 5 and R 6 are substituted by O, SO 0-2 , NR 7 or PO 0-2 R 7 , wherein R 7 and R 8 are identical or different and are H, (C 1 -C 18 )-alkyl, (C 2 -C 18 )-alkenyl, (C 2 -C 18 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 6 -C 18 )-aryl, (C 1 -C 18 )-heteroaryl, (C 1 -C 8 )-alkyl-(C 6 -C 8 )-aryl, (C 1 -C 8 )-alkyl-(C 1 -C 19 )-heteroaryl, (C 1 -C 8 )-alkyl-(C 3 -C 8 )-cyocloalkyl, and these radicals R 7 and R 8 may be substituted once or more than once by identical or different halogen radicals.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2006
From: BAYER CHEMICALS AG
To: LANXESS DEUTSCHLAND GMBH
Reel/Frame 018463/0687 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2006
From: BAYER CHEMICALS AG
To: LANXESS DEUTSCHLAND GMBH
Reel/Frame 018454/0850 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2005
From: GELLER, THOMAS; GERLACH, ARNE; VIDAL-FERRAN, ANTON; MILITZER, HANS-CHRISTIAN; LANGER, REINHARD
To: BAYER CHEMICALS AG
Reel/Frame 015616/0739 →