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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957311Generated: November 3, 2026

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

https://huagongshe.com/reaction/1957311

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 numberUS05783705
Source datasetuspto-grants-1998_07
ORD IDord-051eed2c04774b878ab066978597436f
Source noteuspto-grants-1998_07