IP Library Patent Application 10533010
Patent Application
App. No. 10/533,010

Phthalimidyl-azo dyes, process for their preparation and their use

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Quick Facts
Patent No.
US None
App. No.
10/533,010
Abstract

The present invention relates to dyes of formula (I) wherein R 1 , is 2-methoxyethyl, 2-ethoxyethyl or 2-(2-ethoxyethoxy)ethyl, R 2 is C 1, -C 6 alkyl which is unsubstituted or substituted by one or more hydroxy groups, halogen atoms, C 1, -C 4 alkoxy groups, C 2 -C 8 alkoxyalkoxy groups, C 1, -C 4 alkyl-COO— groups or C 1, -C 4 alkyl-OCO— groups, R 3 is methyl, hydroxy, halogen, —NH—SO 2 —R 5 or —NH—CO—R 6 , wherein R 5 is methyl or ethyl and R 6 is methyl, ethyl, methoxymethyl or 2-methoxyethyl, and R 4 is ethyl or n-propyl, and also to a process for their preparation and to their use in the dyeing or printing of semi-synthetic and, especially, synthetic hydrophobic fibre materials, more especially textile materials.

Claims (21)

1 . A dye of formula

wherein R 1 is 2-methoxyethyl, 2-ethoxyethyl or 2-(2-ethoxyethoxy)ethyl,

R 2 is C 1 -C 6 alkyl which is unsubstituted or substituted by one or more hydroxy groups, halogen atoms, C 1 -C 4 alkoxy groups, C 2 -C 8 alkoxyalkoxy groups, C 1 -C 4 alkyl-COO— groups or C 1 -C 4 alkyl-OCO— groups R 3 is methyl, hydroxy, halogen, —NH—SO 2 —R 5 or —NH—CO—R 6 , wherein R 5 is methyl or ethyl and R 6 is methyl, ethyl, methoxymethyl or 2-methoxyethyl, and

R 4 is ethyl or n-propyl.

2 . A dye according to claim 1 , wherein R 1 and R 2 are the same.

3 . A dye according to claim 1 , wherein R 1 is 2-methoxyethyl.

4 . A dye according to claim 1 , wherein R 3 is —NH—CO—R 6 .

5 . A dye according to claim 4 , wherein R 6 is methyl.

6 . A dye according to claim 1 , wherein R 4 is ethyl.

7 . A dye of formula (1a), (1b) or (1c) according to claim 1

8 . A process for the preparation of a dye of formula (1) according to claim 1 , in which a phthalimide of formula

wherein R 4 is as defined in claim 1 ,

is nitrated in the acidic range, the resulting nitro compound is then alkylated and converted by means of reductive treatment into an intermediate of formula

the intermediate of formula (3) is monohalogenated in an acidic medium and then diazotised, coupled to a compound of formula (4)

wherein R 1 , R 2 and R 3 are as defined in claim 1 , and then the halogen substituent is replaced by cyano.

9 . A dye mixture comprising at least two structurally different dyes of formula (1) according to claim 1 .

10 . A method of dyeing or printing a semi-synthetic or synthetic hydrophobic fibre material, in which a dye of formula (1) according to claim 1 is applied to the mentioned material or incorporated therein.

11 . (canceled)

12 . A semi-synthetic or, synthetic hydrophobic fibre material, which has been dyed or printed by the process according to claim 10 .

13 . A method of dyeing or printing a semi-synthetic or synthetic hydrophobic fibre material, in which a dye mixture according to claim 9 is applied to the mentioned material or incorporated therein.

14 . A semi-synthetic or synthetic hydrophobic textile fibre material which has been dyed or printed by the process according to claim 10.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2007
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 019140/0871 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2006
From: CLEMENT, ANTOINE; ARQUINT, ALFONS; LAUK, URS
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 017597/0857 →