反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]2[CH:13]([C:14](OC)=[O:15])[CH2:12][C:11](=[O:18])[N:10]2[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:6]=[CH:7][CH:8]=1.[BH4-].[Na+]>CO>[OH:15][CH2:14][CH:13]1[CH:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[CH:4]=2)[N:10]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:11](=[O:18])[CH2:12]1参加物
4
実験手順
To 26.7 gm. of methyl 2-(3-methoxyphenyl)-5-oxo-1-phenylpyrrolidin-3-carboxylate in 200 ml of absolute methanol was added slowly at 0°-10° 24.8 gm. of sodium borohydride. The reaction was run and worked up following the procedure of example 1D. Drying (Na2SO4), filtration, and concentration in vacuo provided 17.2 gm. of colorless crystals, m.p. 123°-126°.
後処理
- customDrying
- filtration(Na2SO4), filtration, and concentration in vacuo
- customprovided 17.2 gm
出典と根拠
- ORDレコード
- ord-72fa67b9f4c241e4af330b89a58efc1c
- 出典データセット
- uspto-grants-1987_01
- 特許番号
- US04639529
関連ノート
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