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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236696Generated: November 1, 2026

Hydrochloric Acid → 1,3-Benzodioxole, 5-(chloromethyl)-

https://huagongshe.com/reaction/236696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantPiperonalHCID 8438—
Reactant1,3-BenzodioxoleHCID 9229—
CatalystZincchlorideHCID 3007855—
Product1,3-Benzodioxole, 5-(chloromethyl)-HCID 8871370%

Reaction Steps

A typical process for preparing piperonal from 1,2-methylenedioxybenzene has been reported by P. P. Shorygin et al. [J. Gen. Chem. (U.S.S.R.), 8,975 (1938)]. This is a two-step process. In the first step, 1,2-methylenedioxybenzene is reacted with formalin in petroleum benzine under the influence of hydrogen chloride gas and zinc chloride to form piperonyl chloride (with a 70-78% yield based on the amount of 1,2-methylenedioxybenzene having reacted). This is followed by the second step in which the piperonyl chloride is reacted with an equimolar amount of hexamine in 60% alcohol to give a 70-80% yield of piperonal. By E. D. Laskina et al. [Chemical Abstracts, 57,9714 (1962)], another process has been described in which 1,2-methelenedioxybenzene is reacted with formalin in the presence of a large excess of the sodium salt of m-nitrobenzenesulfonic acid, hydrogen chloride, and an aluminum catalyst to give a 42.4% yield of piperonal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04157333
Source datasetuspto-grants-1979_06
ORD IDord-cae0cf3dbb994694847a15f0c887352c
Source noteuspto-grants-1979_06