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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303688Generated: November 3, 2026

Hydrochloric Acid → 5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole

https://huagongshe.com/reaction/2303688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
Reactant1,3-Benzodioxole, 5-methyl-HCID 81564—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 10559416—

Reaction Steps

To a mixture of methylene chloride (130 L), concentrated HCl (130 L), and tetrabutylammonium bromide (1.61 Kg) was added 5-methylbenzo[d][1,3]dioxole (10 Kg) followed by the slow addition of formaldehyde (14 L, 37 wt % in water). The mixture was stirred overnight. The organic layer was separated, dried with magnesium sulfate and concentrated to an oil. Hexane (180 L) was added and the mixture heated to boiling. The hot hexane solution was decanted from a heavy oily residue and evaporated to give almost pure 5-chloromethyl-6-methylbenzo[d][1,3]dioxole as a white solid. Recrystallization from hexane (50 L) gave 5-chloromethyl-6-methylbenzo[d][1,3]dioxole (80% recovery after recrystallization).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432994B1
Source datasetuspto-grants-2002_08
ORD IDord-79b2a158477b4d14900b1f44496dc898
Source noteuspto-grants-2002_08