IP Library Granted Patent US 7,781,603
Granted Patent B2
US 7,781,603 · App. 11/576,095 · Granted Aug 24, 2010

Method for producing trimethylsilyl azide

Assignee: Toyo Boseki Kabushiki Kaisha
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Quick Facts
Patent No.
US 7,781,603
App. No.
11/576,095
Granted
Aug 24, 2010
Kind
B2
Abstract

The present invention relate to a method for producing a trimethylsilyl azide represented by the formula (3): (CH 3 ) 3 SiN 3   (3) which comprises reacting a trimethylsilyl chloride represented by the formula (1): (CH 3 ) 3 SiCl  (1) with an inorganic salt of hydrogen azide represented by the formula (2): M(N 3 ) n   (2) wherein M represents an alkali metal or an alkaline earth metal, and n represents 1 or 2, in the presence of a phase-transfer catalyst and an organic solvent having a high boiling point.

Claims (48)

1. A method for producing a trimethylsilyl azide represented by the formula (3):

(CH 3 ) 3 SiN 3   (3)

which comprises reacting a trimethylsilyl chloride represented by the formula (1):

(CH 3 ) 3 SiCl  (1)

with an inorganic salt of hydrogen azide represented by the formula (2):

M(N 3 ) n   (2)

wherein M represents an alkali metal or an alkaline earth metal, and n represents 1 or 2, in the presence of a composition consisting of a phase-transfer catalyst and an organic solvent selected from the group consisting of silicon oil, liquid paraffin, dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane, and octadecane.

2. The method according to claim 1 , wherein the inorganic salt of hydrogen azide is sodium azide.

3. The method according to claim 1 , wherein the phase-transfer catalyst is polyethylene glycol or silylated polyethylene glycol.

4. A method for producing a trimethylsilyl azide represented by the formula (3):

(CH 3 ) 3 SiN 3   (3)

which comprises reacting a trimethylsilyl chloride represented by the formula (1):

(CH 3 ) 3 SiCl  (1)

with an inorganic salt of hydrogen azide represented by the formula (2):

M(N 3 ) n   (2)

wherein M represents an alkali metal or an alkaline earth metal, and n represents 1 or 2, in the presence of a composition consisting of a phase-transfer catalyst and an organic solvent;

wherein the organic solvent is a non-polar organic solvent having a boiling point of dodecane or higher.

5. The method according to claim 4 , wherein the organic solvent is silicone oil or liquid paraffin.

6. The method according to claim 4 , wherein the organic solvent is dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane or octadecane.

7. The method according to claim 4 , wherein the inorganic salt of hydrogen azide is sodium azide.

8. The method according to claim 4 , wherein the phase-transfer catalyst is polyethylene glycol or silylated polyethylene glycol.

9. The method according to claim 4 , further comprising isolating the trimethylsilyl azide by a simple distillation.

10. The method according to claim 1 , further comprising isolating the trimethylsilyl azide by a simple distillation.

11. A method for producing a trimethylsilyl azide represented by the formula (3):

(CH 3 ) 3 SiN 3   (3),

the method comprising:

reacting a trimethylsilyl chloride represented by the formula (1):

(CH 3 ) 3 SiCl  (1)

with an inorganic salt of hydrogen azide represented by the formula (2):

M(N 3 ) n   (2); and

isolating the trimethylsilyl azide by a simple distillation;

wherein M represents an alkali metal or an alkaline earth metal, and n represents 1 or 2, in the presence of a phase-transfer catalyst and an organic solvent selected from the group consisting of silicon oil, liquid paraffin, dodecane, tridecane, tetradecane, pentadecane hexadecane, heptadecane, and octadecane.

12. The method according to claim 11 , wherein the inorganic salt of hydrogen azide is sodium azide.

13. The method according to claim 11 , wherein the phase-transfer catalyst is polyethylene glycol or silylated polyethylene glycol.

14. A method for producing a trimethylsilyl azide represented by the formula (3):

(CH 3 ) 3 SiN 3   (3),

the method comprising:

reacting a trimethylsilyl chloride represented by the formula (1):

(CH 3 ) 3 SiCl  (1)

with an inorganic salt of hydrogen azide represented by the formula (2):

M(N 3 ) n   (2); and

isolating the trimethylsilyl azide by a simple distillation;

wherein M represents an alkali metal or an alkaline earth metal, and n represents 1 or 2, in the presence of a phase-transfer catalyst and an organic solvent;

wherein the organic solvent is a non-polar organic solvent having a boiling point of dodecane or higher.

15. The method according to claim 14 , wherein the organic solvent is silicone oil or liquid paraffin.

16. The method according to claim 14 , wherein the organic solvent is dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane or octadecane.

17. The method according to claim 14 , wherein the inorganic salt of hydrogen azide is sodium azide.

18. The method according to claim 14 , wherein the phase-transfer catalyst is polyethylene glycol or silylated polyethylene glycol.

Assignments (2)
MERGER Recorded Jul 8, 2010
From: TOYO KASEI KOGYO COMPANY LIMITED
To: TOYO BOSEKI KABUSHIKI KAISHA
Reel/Frame 024650/0030 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2007
From: KOFUKUDA, TORU; NAKAZAWA, SHIGETO
To: TOYO KASEI KOGYO COMPANY LIMITED
Reel/Frame 019075/0790 →
Priority Claims (1)
JP 2004-317169 · Sep 30, 2004 · national
Continuity (1)
Related Publication 20080058540A1 · Mar 6, 2008