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Hydrochloric Acid → 6,7-Dihydroxy-4-thiaoctanoic acid methyl ester

HRID 1720803
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HRID 1720803 반응식
[O:1]1[CH2:6][CH:2]1[CH:3]([OH:5])[CH3:4].Cl.[SH:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12]>C(Cl)Cl.C[O-].[Na+]>[CH3:14][O:13][C:11](=[O:12])[CH2:10][CH2:9][S:8][CH2:6][CH:2]([OH:1])[CH:3]([OH:5])[CH3:4]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 18050Methyl 3-mercaptopropionateHCID 115934311-(Oxiran-2-yl)ethan-1-ol

생성물 1

HCID 106798886,7-Dihydroxy-4-thiaoctanoic acid methyl ester수율 55%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 10942334Sodium Methoxide용매
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실험 절차

To a solution of 3,4-epoxy-2-butanol as obtained in Reference Example 43 (1.13 g) in methylene chloride (4 ml), methyl 3-mercaptopropionate (2.00 ml) and sodium methylate (260 μl) were added under ice cooling conditions, followed by stirring at room temperature for 1 day. To the reaction mixture, 1N hydrochloric acid was added, and the mixture was extracted with ethyl acetate; the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1) to yield the title compound (1.47 g, yield 55%) as a colorless oily substance.

후처리

  1. additionwere added under ice cooling conditions
  2. extractionthe mixture was extracted with ethyl acetate
  3. distillationthe solvent was distilled off under reduced pressure
  4. customThe resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1)

출처 및 근거

ORD 기록
ord-5de6a0153ba54a78b04b9d334bd4a2b7
출처 데이터셋
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05506267

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