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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250219Generated: October 26, 2026

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

https://huagongshe.com/reaction/250219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDichloromethaneHCID 6344—
Reactant1,3-Benzodioxole, 5-methyl-HCID 81564—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDiethyl EtherHCID 3283—
Product5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 1055941662%

Reaction Conditions

Temperature0 °C

Reaction Steps

At about 0° C., 5-methylbenzo[d][1,3]dioxole (500 mg, 3.68 mmol) and formaldehyde (37% in water, 0.7 mL) were sequentially added to a mixture of dichloromethane (6.8 mL), tetrabutylammonium bromide (80 mg) and concentrated hydrochloric acid (6.5 mL). Under continuous stirring, the mixture was maintained at about 0° C. for about 1 hour and then at ambient temperature for about 4 hours. The mixture was diluted with ether (100 mL). After standard extractive workup, the resulting solid residue was heated with hexanes (100 mL) and the insolubles were removed by filtration. The filtrate was concentrated to give desired product (420 mg, 62%). 1H NMR (300 MHz, CDCl3) δ 6.89 (s, 1H), 6.69 (s, 1H), 5.94 (s, 3H), 4.56 (s, 2H), 2.35 (s, 3H); GC-MS: m/z=184 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863308B2
Source datasetuspto-grants-2011_01
ORD IDord-b6b6d050f2924effa5aa7dbff1654bc5
Source noteuspto-grants-2011_01