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

HCID 24829226, 화합물 → 3-(6-Methoxynaphthalen-2-yl)aniline

HRID 1035603
노트
인쇄 미리보기

반응식

HRID 1035603 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-])=O)[CH:14]=3)[CH:9]=2)[CH:4]=1>C1COCC1.[Pd]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([C:13]1[CH:14]=[C:15]([NH2:19])[CH:16]=[CH:17][CH:18]=1)[CH:7]=[CH:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 24829226HCID 24829226, 화합물

생성물 1

HCID 227240743-(6-Methoxynaphthalen-2-yl)aniline수율 20%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 23938Palladium용매

실험 절차

To a solution of 2-methoxy-6-(3-nitrophenyl)naphthalene (200 mg, 0.71 mmol, 1 eq) in 100 ml of dry THF, Pd/C is added, and the mixture is stirred over night at RT under a hydrogen atmosphere. After filtration over Celite and purification by means of preparative thin-layer chromatograph, the product is obtained in a yield of 20% (36 mg).

후처리

  1. filtrationAfter filtration
  2. customover Celite and purification by means of preparative thin-layer chromatograph
  3. customthe product is obtained in a yield of 20% (36 mg)

출처 및 근거

ORD 기록
ord-81d3a3f1c3484e06afbb198bbe71142f
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546392B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트