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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870791Generated: November 3, 2026

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

https://huagongshe.com/reaction/870791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant(2,2-Difluoro-1,3-dioxaindan-5-yl)methanolHCID 12814281—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solventtert-Butyl methyl etherHCID 15413—
Product5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxoleHCID 21992809—

Reaction Conditions

Temperature20 °C

Reaction Steps

(2,2-difluoro-1,3-benzodioxol-5-yl)-methanol (1.0 eq) was dissolved in MTBE (5 vol). A catalytic amount of 4-(N,N-dimethyl)aminopyridine (DMAP) (1 mol %) was added and SOCl2 (1.2 eq) was added via addition funnel. The SOCl2 was added at a rate to maintain the temperature in the reactor at 15 to 25° C. The temperature was increased to 30° C. for 1 hour, and then was cooled to 20° C. Water (4 vol) was added via addition funnel while maintaining the temperature at less than 30° C. After stirring for an additional 30 minutes, the layers were allowed to separate. The organic layer was stirred, and 10% (w/v) aq NaOH (4.4 vol) was added. After stirring for 15 to 20 minutes, the layers were allowed to separate. The organic phase was then dried (Na2SO4), filtered, and concentrated to afford crude 5-chloromethyl-2,2-difluoro-1,3-benzodioxole that was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969574B2
Source datasetuspto-grants-2015_03
ORD IDord-67879fba7d594d34a5e75bb654b59bf3
Source noteuspto-grants-2015_03