Reaktion #67722

Reaktionsgleichung

Thionyl chloride

(2,2-difluoro-benzo[1,3]dioxol-5-yl)-methanol

→

5-chloromethyl-2,2-difluoro-benzo[1,3]dioxole

Ausbeute 56.1%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeevaporated to dryness
2. 2
   SonstigeThe residue was partitioned between an aqueous solution of saturated sodium bicarbonate (100 mL) and dichloromethane (100 mL)
3. 3
   ExtraktionThe separated aqueous layer was extracted with dichloromethane (150 mL)
4. 4
   Trocknenthe organic layer was dried over sodium sulfate
5. 5
   Filtrationfiltrated
6. 6
   Sonstigeevaporated to dryness

Vorschrift

Thionyl chloride (45 g, 38 mmol) was slowly added to a solution of (2,2-difluoro-benzo[1,3]dioxol-5-yl)-methanol (7.2 g, 38 mmol) in dichloromethane (200 mL) at 0° C. The resulting mixture was stirred overnight at room temperature and then evaporated to dryness. The residue was partitioned between an aqueous solution of saturated sodium bicarbonate (100 mL) and dichloromethane (100 mL). The separated aqueous layer was extracted with dichloromethane (150 mL) and the organic layer was dried over sodium sulfate, filtrated, and evaporated to dryness to give crude 5-chloromethyl-2,2-difluoro-benzo[1,3]dioxole (4.4 g) which was used directly in the next step.

Quelle