反応式
[C:1]1([C@H:7]([NH2:16])[C@H:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CO.[OH:19][CH:20]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:21](=[N:28][OH:29])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C1C=CC=CC=1>[C:10]1([C@H:8]([NH2:9])[C@H:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[NH2:16])[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1.[OH:19][CH:20]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:21](=[N:28][OH:29])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1参加物
5
実験手順
0.934 g (4.40 mmol) of (1S,2S)-(-)-1,2-diphenylethylenediamine of α!D20 =-103.1° (c 1.00, MeOH ) and 1.00 g (4.40 mmol) of dl-1-hydroxy-2-hydroxyimino-1,2-diphenylethane were added to 3 ml of benzene and then heated and stirred, and the solution was cooled to room temperature. Afterward, the precipitated crystals were collected by filtration and then recrystallized from 2 ml of benzene once to obtain 0.250 g of (1S,2S)-(-)-1,2-diphenylethylenediamine·1-hydroxy-2-hydroxyimino-1,2-diphenylethane. Physical properties of the product are as follows.
後処理
- temperatureheated
- filtrationAfterward, the precipitated crystals were collected by filtration
- customrecrystallized from 2 ml of benzene once
出典と根拠
- ORDレコード
- ord-a9601509502d433ba9f8767dcd2a28f4
- 出典データセット
- uspto-grants-1996_04
- 特許番号
- US05510520
関連ノート
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