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.[Cl:22][CH:23]([Cl:27])[C:24](Cl)=[O:25]>O>[CH3:7][C:8]1([CH3:14])[N:12]([C:24](=[O:25])[CH:23]([Cl:27])[Cl:22])[CH2:11][CH:10]([CH3:13])[O:9]1参加物
6
実験手順
Eighteen (18) milliliters of a benzene solution containing 4.6 g. of 2,2,5-trimethyl oxazolidine was added to 25 ml. of benzene and 4.5 g. of triethylamine. Five and nine-tenths (5.9 g.) grams of dichloroacetyl 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 benzene removed under vacuum. Yield was 7.7 g. of an oil, nD30 =1.4950.
後処理
- temperaturecooling in an ice bath
- customWhen reaction
- customthe benzene layer separated
- dry with materialdried over anhydrous magnesium sulfate
- customthe benzene removed under vacuum
出典と根拠
- ORDレコード
- ord-9214ad9ac66d41068cbc5b59c9d0433c
- 出典データセット
- uspto-grants-1980_11
- 特許番号
- US04236011
関連ノート
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