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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651803Generated: October 31, 2026

Piperonal → HCID 23050471, compound

https://huagongshe.com/reaction/1651803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperonalHCID 8438—
ReactantMethyl propiolateHCID 13536—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23050471HCID 23050471—

Reaction Steps

A solution of 5 ml (60 mmol) of methyl propiolate in 60 ml of tetrahydrofuran was treated at -78° under argon with 37.5 ml of n-butyllithium (1.6M in hexane). The mixture was stirred at -78° for 10 minutes and then a solution of 9 g 60 mmol) of 3,4 -methylenedioxybenzaldehyde in 60 ml of tetrahydrofuran was added within 30 minutes. The reaction mixture was stirred at -78° for a further 20 minutes, then brought to room temperature and treated with 80 ml of saturated ammonium chloride solution. The aqueous phase was extracted twice with ether. The combined organic phases were washed in succession with saturated sodium chloride solution and with water, dried over sodium sulphate and concentrated. The residue was purified by flash chromatography on 500 g of silica gel (elution agent methylene chloride/ethyl acetate 9:1). There was obtained methyl 4-hydroxy-4-[3,4-(methylenedioxy) phenyl]-2-butynoate as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929741
Source datasetuspto-grants-1990_05
ORD IDord-ae8b61d84d2b459c9f807d23b06a7937
Source noteuspto-grants-1990_05