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

Sodium Hydroxide → 2-phenyl-1H-indol-3-amine

HRID 746818
노트
인쇄 미리보기

반응식

HRID 746818 반응식
[N:1]([C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[NH:5][C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=O.[OH-].[Na+].S(S([O-])=O)([O-])=O.[Na+].[Na+]>C(O)C>[NH2:1][C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[NH:5][C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24489Sodium DithioniteHCID 3439763-nitroso-2-phenyl-1H-indole

생성물 1

HCID 27493402-phenyl-1H-indol-3-amine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 3-nitroso-2-phenyl indole (28) (25 gm, 0.129 mol) in ethanol (450 ml) was added 2N sodium hydroxide (300 mL, 5.0 eq) followed by sodium dithionite (38 g). The reaction was heated at reflux for 5 h, then filtered. The solid was washed with water and dried under vacuum to provide Compound 29 as a yellow solid. Yield=15 g (72.1%). ES-MS: 209.25 (M++1); NMR (DMSO-d6): 7.0 (m, 1H), 7.1 (m, 1H), 7.22 (m, 1H), 7.32 (m, 2H), 7.40 (m, 1H), 7.48 (m, 2H), 7.60 (m, 1H).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 5 h
  3. filtrationfiltered
  4. washThe solid was washed with water
  5. customdried under vacuum

출처 및 근거

ORD 기록
ord-6f7094c3f70e47c8b959d1b7a0cbfc57
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07393955B2

반응 노트

불러오는 중…