反应 #46060

ord-bd67b92e946446cd96d7efddfc3592d5

反应方程式

O=C([O-])O.[Na+]
sodium bicarbonate
CC(C)(CO)CO
neopentyl glycol
O=C(CCl)CCl
1,3-dichloroacetone
c1ccccc1
benzene
CC1(C)COC(CCl)(CCl)O1
2,2-bis-chloromethyl-5,5-dimethyl-1,3-dioxolane
收率 34.6%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他This compound was synthesized
  2. 2
    干燥The organic layer was dried over anhydrous magnesium sulfate
  3. 3
    浓缩concentrated in vacuo

实验过程

This compound was synthesized by substantially following the procedure of the above-mentioned article by Isaka, Ejiri, and Nakamura. 69 grams of neopentyl glycol, 76 grams of 1,3-dichloroacetone, 50 ml of benzene, and 2.3 g of p-toluenesulfonic acid were refluxed through a Dean-Stark water separator for 8 hours whereon the reaction was diluted with hexanes and neutralized with aqueous sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo yielding 41.2 g of 2,2-bis-chloromethyl-5,5-dimethyl-1,3-dioxolane, a pale yellow liquid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07741245B2uspto-grants-2010_06