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Acetyl isothiocyanate → 3-(3-Acetylthioureido)-4-aminobenzophenone

HRID 1439782
노트
인쇄 미리보기

반응식

HRID 1439782 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][C:15]=1[NH2:16])[C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6].[C:17]([N:20]=[C:21]=[S:22])(=[O:19])[CH3:18]>C(OCC)C>[C:17]([NH:20][C:21](=[S:22])[NH:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][C:15]=1[NH2:16])[C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6])(=[O:19])[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 128851Acetyl isothiocyanateHCID 1355203,4-Diaminobenzophenone

생성물 1

HCID 130231783-(3-Acetylthioureido)-4-aminobenzophenone수율 85%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a stirred solution of 3,4-diaminobenzophenone (8.48 g.; 0.04 mole) in ethyl ether (1.0 L.) there is added dropwise acetyl isothiocyanate (4.04 g.; 0.04 mole). The solution is stirred at room temperature for two hours and a precipitate collected by filtration and dried to afford 10.7 g. (85% yield) of 3-(3-acetylthioureido)-4-aminobenzophenone, m.p. 211° C., dec.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationa precipitate collected by filtration
  2. customdried
  3. customto afford 10.7 g

출처 및 근거

ORD 기록
ord-02660629ce50484bb21c49b4d70c9610
출처 데이터셋
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04060636

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