Decylamine → trans-N-Decyl-2-(4-nitrophenyl)cyclopropanecarboxamide

HRID 1065825

Reaction equation

HRID 1065825 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C@@H:10]2[CH2:12][C@H:11]2[C:13]([OH:15])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:16]([NH2:26])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>>[CH2:16]([NH:26][C:13]([C@@H:11]1[CH2:12][C@H:10]1[C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=1)=[O:15])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]

Participants

3

Reactant 2

HCID 8916DecylamineHCID 12854631rac-(1R,2R)-2-(4-nitrophenyl)cyclopropane-1-carboxylic acid

Product 1

HCID 12854652trans-N-Decyl-2-(4-nitrophenyl)cyclopropanecarboxamideYield 98%

Procedure

The title compound was prepared from trans-2-(4-nitrophenyl)cyclopropanecarboxylic acid and decylamine, substantially according to the procedure of Preparation 30. A 98% yield of a white, waxy solid, m.p. 127°-129° C., was obtained.

Workup

  1. customsubstantially according to the procedure of Preparation 30
  2. customA 98% yield of a white, waxy solid, m.p. 127°-129° C., was obtained

Sources & evidence

ORD record
ord-eb9e00f8f64c4845a774ced8e4913798
Source dataset
uspto-grants-1982_05
Patent number
US04331683

Linked notes

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