IP Library Granted Patent US 8,927,756
Granted Patent B2
US 8,927,756 · App. 13/630,915 · Granted Jan 6, 2015

Method for producing carbamate compound, carbamate compound, and method for producing isocyanate compound using same

Inventors: Takashi Okazoe (Tokyo, JP); Yuko Nagasaki (Tokyo, JP); Hidekazu Okamoto (Tokyo, JP)
Assignee: Asahi Glass Company, Limited
C07C271/20C07C271/24C07C2101/14C07C263/04C07C269/04
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Quick Facts
Patent No.
US 8,927,756
App. No.
13/630,915
Granted
Jan 6, 2015
Kind
B2
Abstract

The present invention relates to a method of producing a carbamate compound, comprising reacting a fluorine-containing carbonic diester compound represented by formula (1) and a non-aromatic diamine compound represented by formula (2) without using a catalyst, to thereby produce a carbamate compound represented by formula (3), and a method of producing an isocyanate compound represented by formula (20) from the carbamate compound without using a catalyst, wherein R represents a fluorine-containing monovalent aliphatic hydrocarbon group, and A represents a divalent aliphatic hydrocarbon group, a divalent alicyclic hydrocarbon group or a divalent aromatic-aliphatic hydrocarbon group.

Claims (30)

1. A method of producing a carbamate compound, comprising reacting a fluorine-containing carbonic diester compound represented by formula (1) and a non-aromatic diamine compound represented by formula (2) without using a catalyst, to thereby produce a carbamate compound represented by formula (3):

(wherein, R represents a fluorine-containing monovalent aliphatic hydrocarbon group);

[Chem. 2]

H 2 N-A-NH 2   (2)

(wherein, A represents a divalent aliphatic hydrocarbon group, a divalent alicyclic hydrocarbon group or a divalent aromatic-aliphatic hydrocarbon group); and

(wherein, R represents a fluorine-containing monovalent aliphatic hydrocarbon group, and A represents a divalent aliphatic hydrocarbon group, a divalent alicyclic hydrocarbon group or a divalent aromatic-aliphatic hydrocarbon group).

2. The method of producing a carbamate compound according to claim 1 , wherein R of formula (1) has no fluorine atom on the α-position carbon atom bonded to the oxygen atom of the carbonate bond, and has two or more groups, in total, of at least one member selected from the group consisting of a fluorine atom, a polyfluoroalkyl group and a perfluoroalkyl group bonded to the adjacent β-position carbon atom.

3. The method of producing a carbamate compound according to claim 1 , wherein R of formula (1) is any of:

2,2,3,3-tetrafluoro-n-propyl group,

2,2,3,3,3-pentafluoro-n-propyl group,

1,1,1,3,3,3-hexafluoro-i-propyl group,

2,2,3,3,3,4,4,5,5-octafluoro-n-pentyl group,

2,2,3,4,4,4-hexafluoro-n-butyl group, or

2,2,2-trifluoroethyl group.

4. The method of producing a carbamate compound according to claim 1 , wherein the non-aromatic diamine compound represented by formula (2) is any of:

1,6-hexamethylenediamine,

isophoronediamine,

1,3-bis(aminomethyl)cyclohexane,

1,4-bis(aminomethyl)cyclohexane,

4,4′-diamino(dicyclohexylmethane),

2,5-bis(aminomethyl)bicyclo[2,2,1]heptane,

2,6-bis(aminomethyl)bicyclo[2,2,1]heptane,

1,3-bis(aminomethyl)benzene, or

1,4-bis(aminomethyl)benzene.

5. A method of producing an isocyanate compound, which comprises:

a step of producing a carbamate compound represented by formula (3), by the method of producing a carbamate compound of claim 1 ; and

a step of producing an isocyanate compound represented by formula (20) from the obtained carbamate compound without using a catalyst:

[Chem. 20]

O═C═N-A-N═C═O  (20)

(wherein, A represents a divalent aliphatic hydrocarbon group, a divalent alicyclic hydrocarbon group or a divalent aromatic-aliphatic hydrocarbon group).

Assignments (2)
CHANGE OF NAME Recorded Aug 7, 2018
From: ASAHI GLASS COMPANY, LIMITED
To: AGC INC.
Reel/Frame 046730/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2012
From: OKAZOE, TAKASHI; NAGASAKI, YUKO; OKAMOTO, HIDEKAZU
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 029049/0514 →
Priority Claims (1)
JP 2010-086126 · Apr 2, 2010 · national
Continuity (2)
Continuation PCTJP2011056095 · Mar 15, 2011
Related Publication 20130023691A1 · Jan 24, 2013