Hydrochloric Acid → 2-(3-Bromophenyl)propan-2-ol
反応式
[CH3:1][Mg]Br.[CH3:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Br:13])[CH:8]=1)=[O:6].O.Cl>C(OCC)C>[Br:13][C:9]1[CH:8]=[C:7]([C:5]([OH:6])([CH3:1])[CH3:4])[CH:12]=[CH:11][CH:10]=1参加物
6
実験手順
To a stirred solution of methylmagnesium bromide (60 mL of a 3.0 M solution in diethyl ether) at 0° C. was added dropwise a solution of 3-bromoacetophenone (29.8 grams) in 75 mL of diethyl ether. Once the addition was complete, the mixture was stirred for 0.5 hours and poured into water. The aqueous phase was acidified with 1M hydrochloric acid and extracted with three portions of diethyl ether. The combined ether layers were washed with saturated sodium bicarbonate, concentrated to afford 30.4 grams of the title compound. 1H NMR δ7.72 (br s, 1), 7.49 (d, 1, J=7.8), 7.37 (d, 1, J=7.9), 7.25 (dd, 1, J=7.8, 7.9), 4.19 (s, 1), 1.50 (br s, 6).
後処理
- additionOnce the addition
- extractionextracted with three portions of diethyl ether
- washThe combined ether layers were washed with saturated sodium bicarbonate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-0df5965ff49c4ffdb52213cbd0310d10
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06166064
反応ノート
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