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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170784Generated: October 30, 2026

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

https://huagongshe.com/reaction/2170784

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051303B2
Source datasetuspto-grants-2015_06
ORD IDord-3f1699c2a004401fb473431b7d1dcce1
Source noteuspto-grants-2015_06