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4-Bromo-2-(1-hydroxy-2-methylpropyl)phenol → 1-(5-Bromo-2-hydroxyphenyl)-2-methylpropan-1-one

HRID 1711789
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HRID 1711789 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([CH:9]([OH:13])[CH:10]([CH3:12])[CH3:11])[CH:3]=1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([C:9](=[O:13])[CH:10]([CH3:11])[CH3:12])[CH:3]=1
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참가 물질

4

반응물 1

HCID 594578434-Bromo-2-(1-hydroxy-2-methylpropyl)phenol

생성물 1

HCID 162206331-(5-Bromo-2-hydroxyphenyl)-2-methylpropan-1-one수율 17%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매2회HCID 6344Dichloromethane용매

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온도
40 °C

실험 절차

4-Bromo-2-(1-hydroxy-2-methylpropyl)phenol (4.88 g, 19.9 mmol) was dissolved in DCM (50 mL) then manganese dioxide (2.44 g, 23.8 mmol) was added. After stirring for about 2 h at ambient temperature another portion of manganese dioxide (2.44 g, 23.8 mmol) was added then the mixture was heated to about 40° C. After about 2 d the mixture was filtered then evaporated and the residue purified by flash chromatography on silica gel with 9:1 Heptane/EtOAc as an eluent to give the title compound (0.82 g, 17%): LC/MS (Table 1, Method a) Rt, =3.38 min; MS m/z: 241.1 (M−H)−.

후처리

  1. additionwas added
  2. filtrationAfter about 2 d the mixture was filtered
  3. customthen evaporated
  4. customthe residue purified by flash chromatography on silica gel with 9:1 Heptane/EtOAc as an eluent

출처 및 근거

ORD 기록
ord-f53cc1705ad14a00a86ea024727b0fa1
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790741B2

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