Water → 4-Bromo-6-isobutyl-benzo[1,3]dioxole

HRID 460310

反応式

HRID 460310 の反応式
[Br:1][C:2]1[C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=[C:4]([CH:11](O)[CH:12]([CH3:14])[CH3:13])[CH:3]=1.C([SiH](CC)CC)C.FC(F)(F)C(O)=O.O>ClCCl>[Br:1][C:2]1[C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=[C:4]([CH2:11][CH:12]([CH3:14])[CH3:13])[CH:3]=1

参加物

6

反応条件

温度
0 °C

実験手順

To a cold solution (0° C.) of 1-(7-bromo-benzo[1,3]dioxol-5-yl)-2-methyl-propan-1-ol (498 mg, 1.82 mmol) in dry dichloromethane (10 mL) was added triethylsilane (0.6 mL, 3.65 mmol). After 15 minutes, trifluoroacetic acid was added to the reaction and the mixture stirred at 0° C. for 45 minutes. Water was poured into the reaction mixture and the layers separated. The organic layer was further washed with water, aqueous NaHCO3 and brine, dried (MgSO4), filtered and evaporated. The residue was purified on silica gel (5% ethyl acetate in hexane) to give 242 mg of 4-bromo-6-isobutyl-benzo[1,3]dioxole (52%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6H), 1.81 (m, 1H), 2.39 (d, J=7.5 Hz, 2H), 6.01 (s, 2H), 6.58 (s, 1H), 6.76 (s, 1H).

後処理

  1. customthe layers separated
  2. washThe organic layer was further washed with water, aqueous NaHCO3 and brine
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was purified on silica gel (5% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-6fcf7cb8bdb94600a5a6b80f990952fd
出典データセット
uspto-grants-2007_03
特許番号
US07196108B2

関連ノート

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