홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(Z)-2-amino-6-(prop-1-enyl)benzonitrile → 2-Amino-6-n-propylbenzonitrile

HRID 711745
노트
인쇄 미리보기

반응식

HRID 711745 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6](/[CH:10]=[CH:11]\[CH3:12])[C:3]=1[C:4]#[N:5]>CCO.[Pd]>[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][CH2:11][CH3:12])[C:3]=1[C:4]#[N:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67399331(Z)-2-amino-6-(prop-1-enyl)benzonitrile

생성물 1

HCID 673998302-Amino-6-n-propylbenzonitrile수율 96%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

(Z)-2-Amino-6-(prop-1-enyl)benzonitrile (Example 131b) (0.45 g, 2.82 mmol) and 10% Pd/C (0.17 g) were stirred in EtOH (15 mL) under a hydrogen atmosphere for 4 h. The catalyst was filtered out, and the organic layer was concentrated under vacuum to give 0.43 g (96%) of 2-amino-6-n-propylbenzonitrile as yellow oil, which was used without further purification. MS 161 (MH+).

후처리

  1. filtrationThe catalyst was filtered out
  2. concentrationthe organic layer was concentrated under vacuum

출처 및 근거

ORD 기록
ord-300ef2b7a1b840a19b58dc55ee2c224b
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181276B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트