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Diethyl Ether → 3-Phenylquinolin-2-thione

HRID 1903216
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반응식

HRID 1903216 반응식
Cl[C:2]1[C:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.NC(N)=[S:20].C(OCC)C>C(O)C>[C:12]1([C:11]2[C:2](=[S:20])[NH:3][C:4]3[C:9]([CH:10]=2)=[CH:8][CH:7]=[CH:6][CH:5]=3)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 2723790ThioureaHCID 42560782-Chloro-3-phenylquinoline

생성물 1

HCID 132002063-Phenylquinolin-2-thione

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 2-chloro-3-phenylquinoline (3.4 g.) and thiourea (1.2 g.) in ethanol (20 ml.) was refluxed for one hour. The solution was allowed to cool to ambient temperature and diethyl ether (10 ml.) was added. The solid which precipitated was filtered off, dispersed in M-sodium hydroxide (70 ml.), and heated on a steam bath for 2 hr. The reaction mixture was acidified with 2 M-hydrochloric acid. The resulting mixture was filtered, and the solid residue was stirred with hot ethanol (50 ml.) and filtered. There was thus obtained as the solid residue 3-phenylquinolin-2-thione, m.p. 242°-4°.

후처리

  1. temperaturewas refluxed for one hour
  2. customThe solid which precipitated
  3. filtrationwas filtered off
  4. additiondispersed in M-sodium hydroxide (70 ml.)
  5. temperatureheated on a steam bath for 2 hr
  6. filtrationThe resulting mixture was filtered
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-7477dd82260441f6b87c6158416abdc1
출처 데이터셋
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04435405

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