反応式
[CH3:1][C@H:2]([NH2:11])[C@@H:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>>[CH3:1][C@H:2]([NH2:11])[C@H:3]([OH:10])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1参加物
3
実験手順
61 grams of this salt were split in a manner analogous to that described in example 1. There were obtained 33 grams of L-3-formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid melting at 179° - 180°C.; [α]D20 - 54.4° as well as 26.5 grams of d-phenylpropanolamine.HCl melting point 173°C.; [α]D20 + 33°. From the mother liquor of the racemate splitting by evaporation to dryness and treatment with isopropanolic HCl there were obtained 28 grams (77%) of l-phenylpropanolamine.HCl, melting point 179°C.; [α]D20 - 31.4°.
後処理
- custom[α]D20 + 33°
- customFrom the mother liquor of the racemate splitting by evaporation to dryness and treatment with isopropanolic HCl there
出典と根拠
- ORDレコード
- ord-14fee53e9c514cb1ac088373d509f9f5
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03947464
関連ノート
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