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Water → 4-(3-Chloropropoxy)benzenecarbothioamide

HRID 1710746
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HRID 1710746 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([NH2:12])=O)=[CH:8][CH:7]=1.COC1C=CC(P2(=S)SP(=S)(C3C=CC(OC)=CC=3)[S:24]2)=CC=1.O>C(Cl)(Cl)Cl.C1(C)C=CC=CC=1>[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](=[S:24])[NH2:12])=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 87949Lawesson's reagentHCID 144071764-(3-Chloropropoxy)benzamide

생성물 1

HCID 594574624-(3-Chloropropoxy)benzenecarbothioamide수율 85%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6212Chloroform용매

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온도
85 °C

실험 절차

4-(3-Chloropropoxy)benzamide ax54 (1.0 g, 4.6 mmole, 1 eq) is dissolved in a 1:1 mixture of chloroform and toluene, 2,4-bis-(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide (1.5 g, 3.7 mmole, 0.8 eq) is added. The reaction is stirred overnight at 85° C. Water is then added and the phases are separated. The organic layer is dried over magnesium sulfate and concentrated under reduce pressure. The crude material is purified by chromatography on silicagel (eluent: dichloromethane/methanol/ammonia 98:1.8:0.2) to provide 0.91 g of 4-(3-chloropropoxy)benzenecarbothioamide ax71 as a white solid.

후처리

  1. additionis added
  2. customthe phases are separated
  3. dry with materialThe organic layer is dried over magnesium sulfate
  4. concentrationconcentrated
  5. customThe crude material is purified by chromatography on silicagel (eluent: dichloromethane/methanol/ammonia 98:1.8:0.2)

출처 및 근거

ORD 기록
ord-2904dfb7cc07414faefca94bc5892ed2
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790720B2

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