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Aluminium lithium hydride → 2-Chloro-4-mercaptophenol

HRID 68230
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HRID 68230 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:9]=[C:10]([S:15]C#N)[CH:11]=[CH:12][C:13]=1[OH:14]>O1CCCC1>[Cl:7][C:8]1[CH:9]=[C:10]([SH:15])[CH:11]=[CH:12][C:13]=1[OH:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 596017022-Chloro-4-thiocyanatophenol

생성물 1

HCID 143697432-Chloro-4-mercaptophenol수율 100%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Lithium aluminium hydride (as a 1M solution in tetrahydrofuran, 71.0 ml, 71.0 mmol) was added dropwise to an ice cold solution of 3-chloro-4-hydroxyphenyl thiocyanate (4.20 g, 22.6 mmol) in tetrahydrofuran (100 mL) under nitrogen. The reaction mixture was stirred and allowed to warm to room temperature over 5 hours. The mixture was cooled to 5° C. and quenched with a 1:1 mixture of tetrahydrofuran:water until no more gas evolution was seen. 1N hydrochloric acid solution in water (30 mL) was then added, and the mixture extracted with ethyl acetate (2-fold 70 mL). The combined organic layers were dried (sodium sulphate) and concentrated in vacuo affording a colourless crystalline solid, 100% yield, 3.60 g.

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후처리

  1. temperatureThe mixture was cooled to 5° C.
  2. customquenched with a 1:1 mixture of tetrahydrofuran
  3. addition1N hydrochloric acid solution in water (30 mL) was then added
  4. extractionthe mixture extracted with ethyl acetate (2-fold 70 mL)
  5. dry with materialThe combined organic layers were dried (sodium sulphate)
  6. concentrationconcentrated in vacuo
  7. customaffording a colourless crystalline solid, 100% yield, 3.60 g

출처 및 근거

ORD 기록
ord-80938e306ddf4358b1a02ccf299ce800
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822439B2

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