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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-BenzodioxoleHCID 9229—
ReactantAcetic acid, 2,2-dichloro-, 1,1'-anhydrideHCID 77772—
Reactant6-Methoxyhexanoic acidHCID 15003010—
Solvent1,1-DichloroethaneHCID 6365—
Product4-(6-Methoxyhexanoyl)-1,2-methylenedioxybenzeneHCID 1974522889.5%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05235068
Source datasetuspto-grants-1993_08
ORD IDord-bfb6ebd466954ec98ef724551b776de1
Source noteuspto-grants-1993_08