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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841374Generated: November 2, 2026

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

https://huagongshe.com/reaction/1841374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDichloromethaneHCID 6344—
Reactant2-Methyl-1,3-benzodioxoleHCID 84167—
CatalystTetrabutylammonium BromideHCID 74236—
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 numberUS06683103B2
Source datasetuspto-grants-2004_01
ORD IDord-a8539749e57045f48562d99a5d4e6f99
Source noteuspto-grants-2004_01