Hydrochloric Acid → 2-Propoxyethyl 4-Bromobenzenesulfonate
反応式
[CH2:1]([O:4][CH2:5][CH2:6][OH:7])[CH2:2][CH3:3].C(N(CC)CC)C.[Br:15][C:16]1[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1.Cl>ClCCl.O>[Br:15][C:16]1[CH:21]=[CH:20][C:19]([S:22]([O:7][CH2:6][CH2:5][O:4][CH2:1][CH2:2][CH3:3])(=[O:24])=[O:23])=[CH:18][CH:17]=1参加物
実験手順
To a solution of 2-propoxy-1-ethanol (1.5 g, 14.4 mmol) and triethylamine (2.2 g, 21.6 mmol) in dichloromethane (20 mL) at 0° C. was added 4-bromobenzenesulfonyl chloride (3.86 g, 15.1 mmol) in dichloromethane (10 mL) dropwise over 30 minutes. The reaction was then warmed to room temperature and stirred for 16 hours. The mixture was then poured into water (50 mL) and acidified with 2N aqueous hydrochloric acid (15 mL). The aqueous layer was extracted with dichloromethane and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to give a crude residue. This was purified by column chromatography on silica gel (50 g), eluting with hexane:ethyl acetate (9:3), to give the title compound (2.2 g, 48%) as a colourless oil.
後処理
- extractionThe aqueous layer was extracted with dichloromethane
- dry with materialthe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give a crude residue
- customThis was purified by column chromatography on silica gel (50 g)
- washeluting with hexane:ethyl acetate (9:3)
出典と根拠
- ORDレコード
- ord-c89d7cc853f34728b8f8c96a8a5e393d
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06518282B1
反応ノート
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