Reaktion #46060

ord-bd67b92e946446cd96d7efddfc3592d5

Reaktionsgleichung

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
Ausbeute 34.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThis compound was synthesized
  2. 2
    TrocknenThe organic layer was dried over anhydrous magnesium sulfate
  3. 3
    Einengenconcentrated in vacuo

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741245B2uspto-grants-2010_06