HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990035Generated: October 27, 2026
Hydrochloric Acid → 5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole
https://huagongshe.com/reaction/990035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1,3-Benzodioxole, 5-methyl- | HCID 81564 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole | HCID 10559416 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458805B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-f96273128ff2473a8d676dcd2ff67d22 |
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| Source note | uspto-grants-2002_10 |
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