反応式
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[C:11](Cl)(=[O:21])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].N1C=CC=CC=1>O>[C:11]([O:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1)(=[O:21])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]参加物
5
実験手順
10 Grams of p-hydroxybenzoic acid and 15 g of decanoic acid chloride were stirred at room temperature, and 7.2 g of pyridine was dropwise added. After the mixture was stirred for 1 day, a reaction product was poured into water, and an organic layer was extracted with dichloromethane. The organic layer was washed with 1N hydrochloric acid and dried over anhydrous sodium sulfate, the solvent was distilled off, and then residue was washed with n-hexane and then dried to give a crude end product.
後処理
- extractionan organic layer was extracted with dichloromethane
- washThe organic layer was washed with 1N hydrochloric acid
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off
- washresidue was washed with n-hexane
- customdried
- customto give a crude end product
出典と根拠
- ORDレコード
- ord-c218088b16c541088a933a7606f68c4c
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05723069
関連ノート
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