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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505073Generated: October 30, 2026

Thionyl Chloride → 5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxole

https://huagongshe.com/reaction/1505073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2,2-Difluoro-1,3-dioxaindan-5-yl)methanolHCID 12814281—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxoleHCID 2199280956.1%

Reaction Steps

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, filtered, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216969B2
Source datasetuspto-grants-2015_12
ORD IDord-5ab5f3f761d14d14a6c11d4b9f5f9e37
Source noteuspto-grants-2015_12