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p-Chlorothiophenol → 2-[(4-Chlorophenyl)thio]ethanamine

HRID 2085763
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인쇄 미리보기

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HRID 2085763 반응식
[Na].Br.Br[CH2:4][CH2:5][NH2:6].[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([SH:14])=[CH:10][CH:9]=1>C(O)C>[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([S:14][CH2:4][CH2:5][NH2:6])=[CH:10][CH:9]=1
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참가 물질

5

반응물 3

HCID 7815p-ChlorothiophenolHCID 27742172-Bromoethylamine hydrobromideHCID 5360545Sodium

생성물 1

HCID 27941942-[(4-Chlorophenyl)thio]ethanamine

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
75 °C

실험 절차

A solution of sodium metal (22.5 mg, 0.98 mmol) in ethanol (2.0 mL) was treated with 2-bromoethylamine hydrobromide (100.0 mg, 0.49 mmol) and 4-chlorobenzenethiol (71.0 mg, 0.49 mmol), heated to 75° C. for 18 hours, and concentrated. The concentrate was partitioned between water (2.0 mL) and diethyl ether (5.0 mL) and the organic phase was dried (MgSO4), filtered, and concentrated to provide the desired product. MS (DCI) m/e 188 (M+H)+.

후처리

  1. concentrationconcentrated
  2. customThe concentrate was partitioned between water (2.0 mL) and diethyl ether (5.0 mL)
  3. dry with materialthe organic phase was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0c4e48012eed4e12a60c5a9bb866d614
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06720338B2

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