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1,2-Ethanedithiol → Methyl 3-(3-hydroxyphenyl)-3-methylbutanoate

HRID 1662559
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HRID 1662559 반응식
C[O:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:16])([CH3:15])[CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH:6]=[CH:7][CH:8]=1.C(S)CS.[Cl-].[Al+3].[Cl-].[Cl-]>ClCCCl>[OH:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:16])([CH3:15])[CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH:6]=[CH:7][CH:8]=1
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참가 물질

5

반응물 3

HCID 109021,2-EthanedithiolHCID 6451240Aluminum(III) ChlorideHCID 57705813Methyl 3-(3-methoxyphenyl)-3-methylbutanoate

생성물 1

HCID 57706158Methyl 3-(3-hydroxyphenyl)-3-methylbutanoate수율 98.4%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

To a solution of methyl 3-(3-methoxyphenyl)-3-methylbutanoate 85.E (0.227 g, 1.02 mmol) in 1,2-dichloroethane (10 mL) was added 1,2-ethanedithiol (1.37 mL, 16.3 mmol) followed by aluminum chloride (1.09 g, 8.17 mmol) at 0° C. The reaction mixture was allowed to slowly warm to room temperature over four hours and was then quenched with saturated Rochelle's salt (potassium sodium tartrate) solution. The mixture was extracted (2×50 mL) with DCM. The combined organic layers were washed with water (1×40 mL) and brine (1×40 mL) and dried over magnesium sulfate. The filtrate was concentrated and the residue was purified by medium pressure chromatography (silica, 0 to 30% EtOAc:hexanes) to give methyl 3-(3-hydroxyphenyl)-3-methylbutanoate 85 (0.209 g, 98.3% yield). MS ESI (pos.) m/e: 226.0 (M+H2O)+.

후처리

  1. customwas then quenched with saturated Rochelle's salt (potassium sodium tartrate) solution
  2. extractionThe mixture was extracted (2×50 mL) with DCM
  3. washThe combined organic layers were washed with water (1×40 mL) and brine (1×40 mL)
  4. dry with materialdried over magnesium sulfate
  5. concentrationThe filtrate was concentrated
  6. customthe residue was purified by medium pressure chromatography (silica, 0 to 30% EtOAc:hexanes)

출처 및 근거

ORD 기록
ord-d8f1041ae3da493ebb8cfbf1257ad20c
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08030354B2

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