HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575992Generated: October 28, 2026
Water → 5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxole
https://huagongshe.com/reaction/575992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2,2-Difluoro-1,3-dioxaindan-5-yl)methanol | HCID 12814281 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxole | HCID 21992809 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035072B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8afc6df20a324520ae64e29299d72a0f |
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| Source note | uspto-grants-2015_05 |
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