HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254329Generated: October 25, 2026
1,3-Benzodioxole → 4-(6-Methoxyhexanoyl)-1,2-methylenedioxybenzene
https://huagongshe.com/reaction/2254329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Benzodioxole | HCID 9229 | — |
| Reactant | Acetic acid, 2,2-dichloro-, 1,1'-anhydride | HCID 77772 | — |
| Reactant | 6-Methoxyhexanoic acid | HCID 15003010 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-(6-Methoxyhexanoyl)-1,2-methylenedioxybenzene | HCID 19745228 | 89.5% |
Reaction Steps
In 50 ml of dichloroethane were dissolved 7.31 g (0.05 mole) of 6-methoxy hexanoic acid and 14.39 g (0.06 mole) of dichloroacetic anhydride. To the resulting solution were added 7.93 g (0.065 mole) of methylenedioxybenzene and 0.71 g of boron trifluoridediethyl ether complex and the resulting mixture was then stirred at 70° C. for 6 hours. After completion of the reaction, the reaction solution was cooled and washed with 5% aqueous sodium carbonate solution and water in this order. The organic layer was concentrated under reduced pressure to obtain 11.2 g of 4-(6-methoxyhexanoyl)-1,2-methylenedioxybenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05235068 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-bfb6ebd466954ec98ef724551b776de1 |
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| Source note | uspto-grants-1993_08 |
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