Benzoyl isocyanate, 2-methyl- → HCID 53870534, compound

HRID 1588295Notes

Reaction equation

HRID 1588295 reaction equation
[NH:1]=[C:2]1[NH:6][C:5]([C:11]([F:14])([F:13])[F:12])([C:7]([F:10])([F:9])[F:8])[C:4](=[C:15]([F:20])[C:16]([F:19])([F:18])[F:17])[S:3]1.[CH3:21][C:22]1[CH:32]=[CH:31][CH:30]=[CH:29][C:23]=1[C:24]([N:26]=[C:27]=[O:28])=[O:25]>C1(C)C=CC=CC=1>[F:14][C:11]([F:12])([F:13])[C:5]1([C:7]([F:10])([F:9])[F:8])[C:4](=[C:15]([F:20])[C:16]([F:17])([F:18])[F:19])[S:3][C:2]([NH:1][C:27]([NH:26][C:24](=[O:25])[C:23]2[CH:29]=[CH:30][CH:31]=[CH:32][C:22]=2[CH3:21])=[O:28])=[N:6]1

Participants

4

Reactant 2

HCID 12259962Benzoyl isocyanate, 2-methyl-HCID 178508427HCID 178508427, compound

Product 1

HCID 53870534HCID 53870534, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

In toluene (10 ml) was dissolved 2-imino-4,4-bis(trifluoromethyl)-5-(tetrafluoroethylidene)-1,3-thiazolidine (1.0 g), and 2-methylbenzoylisocyanate (0.3 g) which is a starting compound was added thereto and the mixture was stirred at room temperature for 3 hours.

Workup

  1. additionwas added

Sources & evidence

ORD record
ord-75d53b715a5a47fe9d6da2c0411dafc0
Source dataset
uspto-grants-1993_06
Patent number
US05221685

Reaction notes

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