反応式
[CH:1]12[O:7][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6]2.[CH3:8][NH:9][CH3:10].Cl>C1C=CC=CC=1>[CH3:8][N:9]([CH3:10])[C@@H:1]1[CH2:6][CH2:5][CH2:4][CH2:3][C@H:2]1[OH:7]参加物
5
実験手順
This compound was previously prepared from cyclohexene oxide and dimethylamine in benzene at room temperature for 14 days in 95% yield, b.p. 90° (20 mm): J. Chem. Soc., 4835 (1965); or in autoclave: C. A. 67, 63899 d, Rocz. Chem. 41, 541 (1967) b.p. 88° (14 mm); also Bull. Soc. Chim. France, 850 (1947): hydrochloride and resolution reported.
後処理
- custom67, 63899 d, Rocz
出典と根拠
- ORDレコード
- ord-89c4a44e39b04448b933484d36cfabda
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04148914
関連ノート
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