反応式
COC(OC)[CH2:4][N:5]([CH3:10])[C:6](=[O:9])[CH2:7][Cl:8].[CH3:13][CH:14]([OH:18])[CH:15]([OH:17])[CH3:16].C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[CH3:16][CH:15]1[CH:14]([CH3:13])[O:18][CH:4]([N:5]([CH3:10])[C:6](=[O:9])[CH2:7][Cl:8])[O:17]1参加物
反応条件
- 温度
- 110 °C
実験手順
N-(2,2-Dimethoxyethyl)-N-methyl-2-chloroacetamide (97.8 grams; 0.5 mole), 2,3-butanediol (45 grams) and 0.2 grams p-toluenesulfonic acid were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distilling head and condenser. The reaction mixture was heated at about 90° C. to 100° for a period of 5 hours. Little reaction occurred as shown by the absence of methanol distilled. The reaction mixture was then heated at about 110° C., for about 2 hours at atmospheric pressure, then 1 hour at reduced pressure. Under these more rigorous conditions, methanol was formed and was distilled off. At the conclusion of the reaction, the reaction mixture was distilled and the fraction boiling at 127° C. to 130° C. at 0.55 mm Hg was the desired product N-(4,5-dimethyl-1,3-dioxolan-2-yl)-N-methyl-2-chloroacetamide.
後処理
- customfitted with a mechanical stirrer
- distillationthermometer, distilling head and condenser
- temperatureThe reaction mixture was heated at about 90° C. to 100° for a period of 5 hours
- customLittle reaction
- distillationdistilled
- custom1 hour
- customUnder these more rigorous conditions, methanol was formed
- distillationwas distilled off
- customAt the conclusion of the reaction
- distillationthe reaction mixture was distilled
出典と根拠
- ORDレコード
- ord-df5f30e24d8848b2aa8a27dab98251d0
- 出典データセット
- uspto-grants-1982_02
- 特許番号
- US04314840
関連ノート
読み込み中…