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

1-Nitro-4-((E)-styryl)-benzene → 4-Aminostilbene

HRID 2072335
노트
인쇄 미리보기

반응식

HRID 2072335 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[CH:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=1)([O-])=O.[H][H]>C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7](/[CH:10]=[CH:11]/[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 980011-Nitro-4-((E)-styryl)-benzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 12727884-Aminostilbene수율 91.1%

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
120 °C

실험 절차

38 g of 4-nitrostilbene are hydrogenated in 120 g of ethanol with 6 g of a CoSx paste prepared according to Example 1, which was digested with ethanol and contains approx. 30% of CoSx, in a stainless steel stirred autoclave at 115° C under 80 bars of H2. The calculated amount of hydrogen for the reduction of the nitro group has been take up within 1 hour. The mixture is stirred for a further 10 minutes at 120° C and 80 bars of H2. The reduction mixture is filtered and the resulting solution gives 30 g of 4-amino-trans-stilbene; melting point 151° C.

후처리

  1. customprepared
  2. customat 115° C
  3. filtrationThe reduction mixture is filtered

출처 및 근거

ORD 기록
ord-b7fb4e27d98042f785fe484621b4fcda
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04051177

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트