Methanimidamide, N,N-diphenyl- → 2-(3-Bromobenzoyl)-3-phenylaminoacrylonitrile

HRID 429350

반응식

HRID 429350 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[C:5]([CH2:7][C:8]#[N:9])=[O:6].[C:13]1([N:19](C2C=CC=CC=2)[CH:20]=N)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C1(C)C(C)=CC=CC=1.CCOCC>[Br:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[C:5]([C:7](=[CH:20][NH:19][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:8]#[N:9])=[O:6]

참가 물질

5

반응물 2

HCID 78296Methanimidamide, N,N-diphenyl-HCID 27568393-(3-Bromophenyl)-3-oxopropanenitrile

생성물 1

HCID 696866072-(3-Bromobenzoyl)-3-phenylaminoacrylonitrile수율 74.3%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 7237O-Xylene용매

실험 절차

A mixture of 2-(3-bromobenzoyl)acetonitrile (16.5 g, 73.6 mmol) and N,N-diphenylformamidine (14.5 g, 73.6 mmol) in xylene (100 ml) was heated at reflux under a nitrogen atmosphere. After 3 h, the reaction mixture was cooled to room temperature and diluted with ether to give 2-(3-bromobenzoyl)-3-phenylaminoacrylonitrile (17.9 g) as a solid.

후처리

  1. temperaturewas heated
  2. temperatureat reflux under a nitrogen atmosphere

출처 및 근거

ORD 기록
ord-4e07e7d566e647afa0fd90a248f18e31
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06316466B1

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