IP Library Granted Patent US 7,579,480
Granted Patent B2
US 7,579,480 · App. 10/565,801 · Granted Aug 25, 2009

Alkoxy-(tetrazol-1-yl)benzaldehyde compound and process for producing the same

Assignee: Toyo Kasei Kogyo Company Limited
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Quick Facts
Patent No.
US 7,579,480
App. No.
10/565,801
Granted
Aug 25, 2009
Kind
B2
Abstract

The present invention relates to a process for producing an alkoxy-(tetrazol-1-yl)benzaldehyde compound represented by Formula (2): wherein A 1 is an alkoxy group, and A 2 is a hydrogen atom, alkyl group or fluorine-substituted alkyl group, the process comprising reacting a 1-(alkoxyphenyl)-1H-tetrazole compound represented by Formula (1): wherein A 1 and A 2 are as defined above, with hexamethylenetetramine in a sulfonic acid solvent, followed by hydrolysis. According to the present invention, an alkoxy-(tetrazol-1-yl)benzaldehyde compound can be safely and efficiently produced by formylating a 1-(alkoxyphenyl)-1H-tetrazole compound.

Claims (19)

1. A process for producing an alkoxy-(tetrazol-1-yl)benzaldehyde compound represented by Formula (2):

wherein A 1 is an alkoxy group, and A 2 is a hydrogen atom, alkyl group or fluorine-substituted alkyl group,

the process comprising reacting a 1-(alkoxyphenyl)-1H-tetrazole compound represented by Formula (1):

wherein A 1 and A 2 are as defined above, with hexamethylenetetramine in a sulfonic acid' solvent, followed by hydrolysis.

2. The process according to claim 1 , wherein the sulfonic acid solvent is a mixed solvent of methanesulfonic acid and trifluoromethanesulfonic acid.

3. The process according to claim 1 , wherein hexamethylenetetramine is used in an amount of 1.0 to 3.0 mol per mol of the 1-(alkoxyphenyl)-1H-tetrazole compound.

4. The process according to claim 1 , wherein A 1 is a methoxy group, and A 2 is a hydrogen atom, methyl group, ethyl group or trifluoromethyl group.

5. A process for producing a 4-alkoxy-3-(tetrazol-1-yl)benzaldehyde compound represented by Formula (4):

wherein A 1 is an alkoxy group, and A 2 is a hydrogen atom, alkyl group or fluorine-substituted alkyl group,

the process comprising reacting a 1-(2-alkoxyphenyl)-1H-tetrazole compound represented by Formula (3):

wherein A 1 and A 2 are as defined above, with hexamethylenetetramine in a sulfonic acid solvent, followed by hydrolysis.

6. A process for producing a 2-alkoxy-4-(tetrazol-1-yl)benzaldehyde compound represented by Formula (6):

wherein A 1 is an alkoxy group, and A 2 is a hydrogen atom, alkyl group or fluorine-substituted alkyl group,

the process comprising reacting a 1-(3-alkoxyphenyl)-1H-tetrazole compound represented by Formula (5):

wherein A 1 and A 2 are as defined above, with hexamethylenetetramine in a sulfonic acid solvent, followed by hydrolysis.

7. A process for producing a 2-alkoxy-5-(tetrazol-1-yl)benzaldehyde compound represented by Formula (8):

wherein A 1 is an alkoxy group, and A 2 is a hydrogen atom, alkyl group or fluorine-substituted alkyl group,

the process comprising reacting a 1-(4-alkoxyphenyl)-1H-tetrazole compound represented by Formula (7):

wherein A 1 and A 2 are as defined above, with hexamethylenetetramine in a sulfonic acid solvent, followed by hydrolysis.

Assignments (2)
MERGER Recorded Jul 2, 2010
From: TOYO KASEI KOGYO COMPANY LIMITED
To: TOYO BOSEKI KABUSHIKI KAISHA
Reel/Frame 024651/0023 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2006
From: HAGIYA, KAZUTAKE; SATO, YASUHIRO
To: TOYO KASEI KOGYO COMPANY LIMITED
Reel/Frame 017505/0885 →
Priority Claims (1)
JP 2003-285266 · Aug 1, 2003 · national
Continuity (1)
Related Publication 20070060630A1 · Mar 15, 2007