Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352328Generated: October 31, 2026

Hydrochloric Acid → 2-n-Butyl-3-methoxy-5,6-methylenedioxyindene

https://huagongshe.com/reaction/2352328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant2-n-Butyl-3-(3,4-methylenedioxyphenyl)acrylaldehydeHCID 53730803—
Product2-n-Butyl-3-methoxy-5,6-methylenedioxyindeneHCID 1984423990%

Reaction Steps

Dissolved in 80 ml of methanol was 12 g of 2-n-butyl-3-(3,4-methylenedioxyphenyl)acrylaldehyde, into which hydrogen chloride gas was blown under ice-salt cooling. Upon confirmation of full consumption of the raw material by thin-layer chromatography (eluent: a 5:1 mixture of n-hexane and ether), the bubbling of hydrogen chloride gas was stopped. Water was added to the reaction mixture, followed by extraction of the resultant mixture, followed by extraction of the resultant mixture with ether. After the resultant ether solution was washed with water, a saturated aqueous solution of sodium hydrogencarbonate and water successively, the ether solution was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: a 10:1 mixture of n-hexane and ether) to give 11.4 g of 2-n-butyl-3-methoxy-5,6-methylenedioxyindene as an oily substance (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876345
Source datasetuspto-grants-1989_10
ORD IDord-5d1df5c8071747c79535c090d10c0075
Source noteuspto-grants-1989_10