HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892453Generated: October 28, 2026
Water → 5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxole
https://huagongshe.com/reaction/1892453
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) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507687B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-7d7743c03f2e43c3be37a86e24202f9c |
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| Source note | uspto-grants-2013_08 |
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