Cyclopropylamine → HCID 21413083, compound

HRID 1658949Notes

Reaction equation

HRID 1658949 reaction equation
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.[Cl:5][C:6]1[C:11]([N+:12]([O-:14])=[O:13])=[C:10](Cl)[C:9]([N+:16]([O-:18])=[O:17])=[CH:8][C:7]=1[C:19]([F:22])([F:21])[F:20]>C1CCCCC1>[CH:1]1([NH:4][C:10]2[C:9]([N+:16]([O-:18])=[O:17])=[CH:8][C:7]([C:19]([F:20])([F:21])[F:22])=[C:6]([Cl:5])[C:11]=2[N+:12]([O-:14])=[O:13])[CH2:3][CH2:2]1

Participants

4

Reactant 2

HCID 69828CyclopropylamineHCID 943982,4-Dichloro-1,3-dinitro-5-(trifluoromethyl)benzene

Product 1

HCID 21413083HCID 21413083, compound

Reagents, catalysts & solvents 1

HCID 8078CyclohexaneSolvent

Procedure

The compound was prepared by eacting cyclopropylamine with 2,4-dichloro-3,5-dinitrobenzotrifluoride in cyclohexane to give the product having a melting point of 86° - 87°C.

Workup

  1. customThe compound was prepared
  2. customto give the product

Sources & evidence

ORD record
ord-c98743c9e41d46ebb12e48cc9b236d39
Source dataset
uspto-grants-1976_06
Patent number
US03966816

Reaction notes

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