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Acrylonitrile → 3-[(Cyclopropylmethyl)amino]propanenitrile

HRID 349515
Notes
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Reaction equation

HRID 349515 reaction equation
[C:1](#[N:4])[CH:2]=[CH2:3].[NH2:5][CH2:6][CH:7]1[CH2:9][CH2:8]1>>[CH:7]1([CH2:6][NH:5][CH2:3][CH2:2][C:1]#[N:4])[CH2:9][CH2:8]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 7855AcrylonitrileHCID 75646Cyclopropanemethanamine

Product 1

HCID 183489073-[(Cyclopropylmethyl)amino]propanenitrile

Procedure

With stirring and cooling in an ice-bath to maintain a temperature of 8–10° C., acrylonitrile (0.614 ml) was added to aminomethylcyclopropane (0.651 g). The resultant mixture was stirred at room temperature for 15 h to give the title compound (1.02 g) as a yellow oil.

Workup

  1. temperaturecooling in an ice-bath

Sources & evidence

ORD record
ord-b67c1ed0828f468a8f1f407676f3a4bf
Source dataset
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07179835B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes