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Sodium borohydride → 1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol

HRID 1849964
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HRID 1849964 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][C:10]([C:13](=[O:15])[CH3:14])=[CH:11][N:12]=2)=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:9][C:10]([CH:13]([OH:15])[CH3:14])=[CH:11][N:12]=2)=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 70622881-[2-(4-Chlorophenyl)-1,3-thiazol-5-yl]-1-ethanone

생성물 1

HCID 595624751-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol수율 96.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a stirred solution of 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanone (2.38 g, 10 mmol) in methanol (20 ml) at 0° C. is added sodium borohydride (379 mg, 10.5 mmol) in one portion. The resultant solution is allowed to warm to room temperature, and is then stirred at room temperature for 3 hours. The reaction is quenched with saturated aqueous ammonium chloride solution (200 ml) and extracted with chloroform (200 ml). The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuuo to give desired product as a brown solid (2.32 g)

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후처리

  1. customThe reaction is quenched with saturated aqueous ammonium chloride solution (200 ml)
  2. extractionextracted with chloroform (200 ml)
  3. dry with materialThe organic layer is dried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuuo

출처 및 근거

ORD 기록
ord-0ba5604d72534a50bf49f6905b656d5f
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08956999B2

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