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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039130Generated: November 4, 2026

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

https://huagongshe.com/reaction/1039130

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 15-25° C. The temperature was increased to 30° C. for 1 h, 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 min, 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 min, 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 numberUS08552034B2
Source datasetuspto-grants-2013_10
ORD IDord-0c563145d7fd440892ef20b6f4b9f1a2
Source noteuspto-grants-2013_10