1-(4-(4-Bromophenoxy)phenyl)ethanone → 2-[4-(4-Bromo-phenoxy)-phenyl]-propan-2-ol

HRID 404707

반응식

HRID 404707 반응식
[CH3:1][Mg]Br.[Br:4][C:5]1[CH:20]=[CH:19][C:8]([O:9][C:10]2[CH:15]=[CH:14][C:13]([C:16](=[O:18])[CH3:17])=[CH:12][CH:11]=2)=[CH:7][CH:6]=1>C1COCC1>[Br:4][C:5]1[CH:20]=[CH:19][C:8]([O:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]([OH:18])([CH3:1])[CH3:17])=[CH:12][CH:11]=2)=[CH:7][CH:6]=1

참가 물질

4

반응물 2

HCID 108034801-(4-(4-Bromophenoxy)phenyl)ethanoneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 595717062-[4-(4-Bromo-phenoxy)-phenyl]-propan-2-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A 1.4 M solution of methylmagnesium bromide in THF (7.36 ml; 10.304 mmol) was added to a stirred solution of 4′-(4-bromophenoxy)acetophenone (1 g, 3.435 mmol; [CAS: 54916-27-7]) in THF (40 ml) at 0° C. under a nitrogen atmosphere. The reaction mixture was stirred for 3 hours. The reaction was quenched by the addition of an aqueous solution of saturated ammonium chloride and extracted with EtOAc. The combined organic extracts were dried (Na2SO4) and the solvent was evaporated to dryness. The crude residue was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D28 (0.8 g, 75%).

후처리

  1. customThe reaction was quenched by the addition of an aqueous solution of saturated ammonium chloride
  2. extractionextracted with EtOAc
  3. dry with materialThe combined organic extracts were dried (Na2SO4)
  4. customthe solvent was evaporated to dryness
  5. customThe crude residue was purified by column chromatography (silica gel; DCM as eluent)
  6. customThe desired fractions were collected
  7. customevaporated in vacuo
  8. customto yield intermediate D28 (0.8 g, 75%)

출처 및 근거

ORD 기록
ord-8a68486e3561456682eab521fb7a47bb
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08748621B2

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