反応式
C1C=CC=CC=1.[CH3:7][C:8]1([CH3:14])[NH:12][CH2:11][CH:10]([CH3:13])[O:9]1.C(N(CC)CC)C.[Br:22][CH:23]([CH2:27][Br:28])[C:24](Cl)=[O:25]>O>[CH3:7][C:8]1([CH3:14])[N:12]([C:24](=[O:25])[CH:23]([Br:22])[CH2:27][Br:28])[CH2:11][CH:10]([CH3:13])[O:9]1参加物
6
実験手順
Fourteen milliliters of a benzene solution containing 3.5 g. of 2,2,5-trimethyl oxazolidine was added to 25 ml. of benzene and 3.5 g. of triethylamine. Seven and one-half grams of 2,3-dibromopropionyl chloride was added dropwise with stirring and cooling in an ice bath. When reaction was complete, the mixture was poured into water and the benzene layer separated, dried over anhydrous magnesium sulfate and the solvent stripped under vacuum. The yield was 5.7 g. of an oil, nD30 = 1.5060.
後処理
- temperaturecooling in an ice bath
- customWhen reaction
- customthe benzene layer separated
- dry with materialdried over anhydrous magnesium sulfate
出典と根拠
- ORDレコード
- ord-901566a40ea94522a7749acc58167ccf
- 出典データセット
- uspto-grants-1976_05
- 特許番号
- US03959304
関連ノート
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