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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260675Generated: October 26, 2026

Water → (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/2260675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-Acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuranHCID 19078578—
ReactantHCID 178418244HCID 178418244—
CatalystBenzyltriphenylphosphonium chlorideHCID 70671—
SolventTetrahydrofuranHCID 8028—
Product(Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuranHCID 6767145077.2%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A suspension of benzyltriphenylphosphonium chloride (0.7 g, 1.8 mmol) in tetrahydrofuran (10 ml) was cooled to -20° C. and n-butyllithium hexane solution (1.6 M, 1.12 ml, 1.8 mmol) was added dropwise. The reaction mixture was stirred for 30 minutes and then a solution of 5-acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (0.45 g, 1.7 mmol) in tetrahydrofuran (5 ml) was added. The reaction mixture was stirred at room temperature for additional 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extract was washed with water, dried and then concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1) to obtain the desired compound (0.44 g, yield: 76.2%) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478844
Source datasetuspto-grants-1995_12
ORD IDord-32a609b450604146bd1a44dae91e11f1
Source noteuspto-grants-1995_12