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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Piperonal | HCID 8438 | — |
| Reactant | 1,3-Benzodioxole | HCID 9229 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04157333 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-cae0cf3dbb994694847a15f0c887352c |
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| Source note | uspto-grants-1979_06 |
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