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Boron tribromide → Ethyl 3-hydroxy-4-methylphenylacetate

HRID 516862
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HRID 516862 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:6]=[CH:7][C:8]=1[CH3:9].B(Br)(Br)Br>C(Cl)Cl>[OH:2][C:3]1[CH:4]=[C:5]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:6]=[CH:7][C:8]=1[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 21079756Ethyl 3-methoxy-4-methylphenylacetate

생성물 1

HCID 21079755Ethyl 3-hydroxy-4-methylphenylacetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of Ethyl 2-(3-methoxy-4-methylphenyl)acetate (Step B, 4.12 g, 19.8 mmol) in methylene chloride (30 ml) was added BBr3 (1M in CH2Cl2, 25 ml) at −78° C. under argon, the cold bath was substituted by ice bath after 30 minutes and the reaction mixture was stirred at the same temperature for 2 hours and then 30 minutes at room temperature. The reaction mixture was quenched by addition of ice and worked up by washing with water and brine. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hexane:ethyl acetate, 2:1) to give the title compound.

후처리

  1. custom30 minutes
  2. customat room temperature
  3. customThe reaction mixture was quenched by addition of ice
  4. washby washing with water and brine
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by flash chromatography on a silica gel column (hexane:ethyl acetate, 2:1)

출처 및 근거

ORD 기록
ord-23870f5872ac4f7586898f29e3e68e00
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115072B2

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