2,4-Dichloro-1,3-dinitro-5-(trifluoromethyl)benzene → HCID 21413090, compound

HRID 2071236Notes

Reaction equation

HRID 2071236 reaction equation
[Cl:1][C:2](=[CH2:5])[CH2:3][NH2:4].[Cl:6][C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[C:11](Cl)[C:10]([N+:17]([O-:19])=[O:18])=[CH:9][C:8]=1[C:20]([F:23])([F:22])[F:21]>C(O)C>[Cl:1][C:2](=[CH2:5])[CH2:3][NH:4][C:11]1[C:10]([N+:17]([O-:19])=[O:18])=[CH:9][C:8]([C:20]([F:21])([F:22])[F:23])=[C:7]([Cl:6])[C:12]=1[N+:13]([O-:15])=[O:14]

Participants

4

Procedure

The compound was prepared by reacting 2-chloroallylamine with 2,4-dichloro-3,5-dinitrobenzotrifluoride in ethanol. After recrystallization from ethanol, the compound melts at 78°-80° C.

Workup

  1. customThe compound was prepared
  2. customAfter recrystallization from ethanol

Sources & evidence

ORD record
ord-efdf274d27d74765bb9a5883913e14bb
Source dataset
uspto-grants-1977_09
Patent number
US04046758

Reaction notes

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