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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 3-[(2-Methoxy-2-oxoethyl)thio]butanoic acid

HRID 1360178
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HRID 1360178 반응식
[CH3:1][O:2][C:3](=[O:16])[CH2:4][S:5][CH:6]([CH3:15])[CH2:7][C:8]([O:10]C(C)(C)C)=[O:9].FC(F)(F)C(O)=O>ClCCl>[CH3:1][O:2][C:3](=[O:16])[CH2:4][S:5][CH:6]([CH3:15])[CH2:7][C:8]([OH:10])=[O:9]
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86621910t-Butyl 3-[(2-methoxy-2-oxoethyl)thio]butanoate2회

생성물 1

HCID 436178343-[(2-Methoxy-2-oxoethyl)thio]butanoic acid수율 85%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1.5 g (6.0 mmol) of t-butyl 3-[(2-methoxy-2-oxoethyl)thio]butanoate (product of step 1) was stirred at room temperature with 10 mL of dichloromethane and 5 mL of trifluoroacetic acid for 6 hours, followed by distillation under reduced pressure. After addition of 40 mL of ethylacetoacetate 40 mL and washing with water, an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and then the residue was purified by column chromatography to give 1 g (5.1 mmol) of the title compound in a yield of 85%.

후처리

  1. distillationfollowed by distillation under reduced pressure
  2. additionAfter addition of 40 mL of ethylacetoacetate 40 mL
  3. washwashing with water
  4. dry with materialan organic layer was dried over anhydrous magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-b8086375fb1449a4bfb1e2a03d80a367
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879848B2

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