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tert-Butanol → 1-Bromo-3-tert-butoxy-5-fluorobenzene

HRID 658334
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HRID 658334 반응식
[C:1]([OH:5])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].[F:8][C:9]1[CH:10]=[C:11]([Br:16])[CH:12]=[C:13](F)[CH:14]=1>CC(N(C)C)=O>[Br:16][C:11]1[CH:10]=[C:9]([F:8])[CH:14]=[C:13]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])[CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6386tert-ButanolHCID 24758Sodium hydrideHCID 1363131-Bromo-3,5-difluorobenzene

생성물 1

HCID 568442921-Bromo-3-tert-butoxy-5-fluorobenzene

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매

실험 절차

tert-Butanol (28.2 g) is dissolved in dimethyl acetamide (200 ml). NaH (15.6 g, 60% dispersion in oil) is added over 15 minutes. The reaction mixture is stirred at room temperature for 2 hours. 3,5-difluorobromobenzene (50 g) is added drop wise over 30 minutes. The reaction mixture is stirred at room temperature until shown to be complete by HPLC. The reastion mixture is quenched by addition of water (10 ml), washed with water (1×), dried over MgSO4, filtered and the solvent removed in vacuo to give the title compound. 1H nmr (CDCl3, 400 MHz); 7.00 (ddd, 1H), 6.95 (dd, 1H), 6.68 (ddd, 1H), 1.4 (s, 9H).

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후처리

  1. stirringThe reaction mixture is stirred at room temperature
  2. customThe reastion mixture is quenched by addition of water (10 ml)
  3. washwashed with water (1×)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-101f7ed79d0641a6bef670c3d6da2f2c
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08076489B2

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