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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384159Generated: October 31, 2026

Water → HCID 70223406, compound

https://huagongshe.com/reaction/1384159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl AcrylateHCID 7294—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15428931HCID 15428931—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 70223406HCID 70223406—

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 2 g (4.8 mmol) of 3-iodophenyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)-methanone in 30 ml of DMF is introduced into a three-necked flask under a stream of nitrogen, followed by successive addition of 1.7 g of potassium carbonate, 1.4 g of tetrabutylammonium chloride and 600 μl (6.2 mmol) of methyl acrylate. The reaction medium is degassed by bubbling a stream of argon through it, and 22 mg (0.1 mmol) of palladium acetate are introduced. The reaction medium is heated at 55° C. for six hours and then poured into water, the mixture is extracted with ethyl acetate and the organic phase is separated out after settling has taken place, washed with water, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a mixture of ethyl acetate and heptane (90/10). After evaporation of the solvents, 1.39 g (77%) of the expected methyl ester, with a melting point of 103-4° C., are collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258775B1
Source datasetuspto-grants-2001_07
ORD IDord-6632822968f94db2a8b4846c5d410bf3
Source noteuspto-grants-2001_07