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Trichloromethanethiol → 5-Chloro-3-(2-thienyl)-1,2,4-thiadiazole

HRID 2263344
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HRID 2263344 반응식
Cl.[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7](=[NH:9])[NH2:8].[Cl:10][C:11]([SH:14])(Cl)Cl.[OH-].[Na+]>ClCCl.O>[Cl:10][C:11]1[S:14][N:8]=[C:7]([C:3]2[S:2][CH:6]=[CH:5][CH:4]=2)[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6390TrichloromethanethiolHCID 14798Sodium HydroxideHCID 2781759Thiophene-2-carboximidamide Hydrochloride

생성물 1

HCID 27358235-Chloro-3-(2-thienyl)-1,2,4-thiadiazole수율 69.3%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매
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실험 절차

To a solution of thiophene-2-carboximidamide hydrochloride (1.62 g, 10.0 mmol) and perchloromethyl mercaptan (1.07 ml, 10.0 mmol) in dichloromethane (10 ml) was added dropwise a solution of sodium hydroxide (1.60 g, 40.0 mmol) in water (4 ml) under ice-cooling. Then, the reaction mixture was stirred under ice-cooling for 1 hour and at room temperature for 1 hour. The organic layer was separated, washed with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to give 1.40 g (69.3%) of the desired product as an oil.

후처리

  1. temperaturecooling
  2. customThe organic layer was separated
  3. washwashed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1)

출처 및 근거

ORD 기록
ord-fd0e7c7538ed4e96a5f23d6e22bbcddd
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07851473B2

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