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Toluene → 1-(4-Bromophenyl)-2-methylpropan-2-ol

HRID 713044
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HRID 713044 반응식
Br[Mg]C.[C:4]1(C)C=CC=CC=1.[Br:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18]C(OCC)=O)=[CH:14][CH:13]=1.CC[O:26][CH2:27][CH3:28]>C1COCC1>[Br:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][C:27]([CH3:28])([OH:26])[CH3:4])=[CH:14][CH:13]=1
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참가 물질

6

반응물 4

HCID 1140TolueneHCID 3283Diethyl Ether2회HCID 7020609Ethyl 2-(4-bromophenyl)acetateHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 3167851-(4-Bromophenyl)-2-methylpropan-2-ol수율 73%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
40 °C

실험 절차

A solution of bromo(methyl)magnesium in diethyl ether (25 mL of 3 M, 74.5 mmol) in THF (8 mL) and toluene (25 mL) was added to a solution of ethyl 2-(4-bromophenyl)acetate (8.23 g, 33.9 mmol) in Et2O (165 mL) and the reaction mixture was stirred at 40° C. for 1 hour. The reaction mixture was quenched by the addition of saturated aqueous ammonium chloride (200 mL) and the phases were separated. The organics were dried over sodium sulfate, filtered and concentrated in vacuo. The resulting residue was purified by silica gel column chromatography eluting with 0-30% EtOAc-hexanes to give 1-(4-bromophenyl)-2-methyl-propan-2-ol (5.68 g, 73%), as a clear oil. ESI-MS m/z calc. 228.1. found 229.5 (M+1)+; Retention time: 1.45 minutes (3 min run).

후처리

  1. customThe reaction mixture was quenched by the addition of saturated aqueous ammonium chloride (200 mL)
  2. customthe phases were separated
  3. dry with materialThe organics were dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue was purified by silica gel column chromatography
  7. washeluting with 0-30% EtOAc-hexanes

출처 및 근거

ORD 기록
ord-50a8483d17614887afefbb0b638c147d
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181273B2

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