反応式
C[O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([Cl:10])[C:7]([NH2:11])=[CH:6][C:5]=1[O:12][CH2:13][CH2:14][O:15][CH3:16].[OH-].[Na+].O>C(O)C>[NH2:11][C:7]1[C:8]([Cl:10])=[CH:9][C:4]([C:3]([OH:17])=[O:2])=[C:5]([O:12][CH2:13][CH2:14][O:15][CH3:16])[CH:6]=1参加物
5
実験手順
A solution of the ester (2.75 g, 0.0106 mole) in 95% ethanol (20 ml) was treated with 50% sodium hydroxide (10 ml) and water (10 ml), and refluxed for one hour. The ethanol was removed in vacuo and replaced with water, and the aqueous solution was extracted with ether (20 ml) and adjusted to pH~4 with concentrated hydrochloric acid (16 ml). A solid soon precipitated, and this was filtered, washed with water, air dried, and recrystallized from ethyl acetate (2 crops) to afford 2.03 g (78%) of the title compound as fine pale tan needles; mp 119°-120° C.
後処理
- temperaturerefluxed for one hour
- customThe ethanol was removed in vacuo
- extractionthe aqueous solution was extracted with ether (20 ml)
- customA solid soon precipitated
- filtrationthis was filtered
- washwashed with water, air
- customdried
- customrecrystallized from ethyl acetate (2 crops)
出典と根拠
- ORDレコード
- ord-883d96e6799b4a57ada5dddcba134dae
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05137895
関連ノート
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