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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673126Generated: November 1, 2026

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

https://huagongshe.com/reaction/1673126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2,2-Difluoro-1,3-dioxaindan-5-yl)methanolHCID 12814281—
Product5-(Chloromethyl)-2,2-difluorobenzo[d][1,3]dioxoleHCID 2199280989%

Reaction Steps

A solution of (2,2-difluorobenzo[d][1,3]dioxol-5-yl)methanol (120 g, 0.64 mol) in neat thionyl chloride (500 mL) was stirred for 2 h at 25° C. The excess thionyl chloride was distilled off in vacuo. The residue was partitioned between saturated NaHCO3 (400 mL) and dichloromethane (200 mL). The separated aqueous layer was extracted with dichloromethane (300 mL×3). The combined organic layers were dried, filtered and concentrated in vacuo to give 5-(chloromethyl)-2,2-difluorobenzo[d][1,3]dioxole (117.6 g, 89%), which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999113B2
Source datasetuspto-grants-2011_08
ORD IDord-22c7e25cc7ff42c8a11fafb3d5e4c509
Source noteuspto-grants-2011_08