Hydrochloric Acid → 2,2-Bis(6-benzyloxyhexyl)acetic acid
反応式
[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH:15]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:16]([O:18]CC)=[O:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].Cl>CO>[CH2:28]([O:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH:15]([CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:16]([OH:18])=[O:17])[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1参加物
5
実験手順
First, 12 g of ethyl 2,2-bis(6-benzyloxyhexyl)acetate, 250 ml of methanol, and 100 ml of an aqueous solution containing 16.8 g of 85% potassium hydroxide were placed in a 500 ml flask. Then, the mixture was stirred under reflux for 2 hours. The reaction mixture was poured into diluted hydrochloric acid, and an organic layer was extracted with ether. The ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was recrystallized from a mixed solvent of hexane and acetone to obtain 6.2 g of 2,2-bis(6-benzyloxyhexyl)acetic acid (Y: 55%).
後処理
- customwere placed in a 500 ml flask
- temperatureunder reflux for 2 hours
- extractionan organic layer was extracted with ether
- washThe ether layer was washed with water
- dry with materialdried over anhydrous sodium sulfate
- distillationThereafter, the solvent was distilled away
- customThe residue was recrystallized from a mixed solvent of hexane and acetone
出典と根拠
- ORDレコード
- ord-b8cb1134b8f24782907061084f72bf38
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05750213
反応ノート
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