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Thiourea → 2-[2-(3-Nitrophenyl)cyclohex-1-enylmethyl]isothiourea hydrochloride

HRID 1693153
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인쇄 미리보기

반응식

HRID 1693153 반응식
[NH2:1][C:2]([NH2:4])=[S:3].[Cl:5][CH2:6][C:7]1[CH2:12][CH2:11][CH2:10][CH2:9][C:8]=1[C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-:21])=[O:20])[CH:14]=1>C(O)C>[ClH:5].[N+:19]([C:15]1[CH:14]=[C:13]([C:8]2[CH2:9][CH2:10][CH2:11][CH2:12][C:7]=2[CH2:6][S:3][C:2](=[NH:4])[NH2:1])[CH:18]=[CH:17][CH:16]=1)([O-:21])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 578277541-(2-Chloromethylcyclohex-1-enyl)-3-nitrobenzene

생성물 1

HCID 672787672-[2-(3-Nitrophenyl)cyclohex-1-enylmethyl]isothiourea hydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Thiourea (495 mg) was added to a solution of 1-(2-chloromethylcyclohex-1-enyl)-3-nitrobenzene obtained in Preparation Example 4-(3) (1.56 g) in ethanol (71.6 mL), and the mixture was stirred with heating under reflux for four hours. The reaction solution was cooled to room temperature and then the solvent was evaporated under reduced pressure. The residual solid was washed with ether to obtain the title compound (2.04 g).

후처리

  1. temperaturewith heating
  2. temperatureunder reflux for four hours
  3. customthe solvent was evaporated under reduced pressure
  4. washThe residual solid was washed with ether

출처 및 근거

ORD 기록
ord-8b8475e8850e47d7ac3a2302afc86c97
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158620B2

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