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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303687Generated: October 31, 2026

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

https://huagongshe.com/reaction/2303687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
Reactant1,3-Benzodioxole, 5-methyl-HCID 81564—
SolventDiethyl EtherHCID 3283—
Product5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 1055941663%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 1:1 mixture of ethyl ether (100 ml) and conc. HCl (100 ml) at 0° C. was added (3,4-methylenedioxy)toluene (10 ml). Formaldehyde (20 ml, 37% in water) was then added dropwise. The reaction was stirred at 0° C. for 2 hours and at room temperature for an additional 10 hours. The reaction mixture was then diluted with ethyl ether (100 ml) and the two layers were separated. The organic layer was dried (MgSO4), the solid was filtered and the filtrate was concentrated. The residue was then heated with hexane (200 ml) and the insolubles were filtered off the hot solution. The filtrate was concentrated to give a mixture of (3,4-methylenedioxy)-6-methylbenzyl chloride (9.4 g, 63% yield) and bis[(3,4-methylenedioxy)-6-methyl]phenylmethane (3.6 g) as a white solid. This mixture was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432994B1
Source datasetuspto-grants-2002_08
ORD IDord-050a0826ec3b4facb2d2b7d1a6887c52
Source noteuspto-grants-2002_08