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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267778Generated: October 31, 2026

Water → 7-Methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-one

https://huagongshe.com/reaction/1267778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
Reactant7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-oneHCID 11130368—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product7-Methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-oneHCID 1854628179%

Reaction Conditions

Temperature10 °C

Reaction Steps

Allyl bromide (5.7 ml, 66.56 mmol) was added dropwise to a solution of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (2 g, 6.64 mmol) in dimethyl sulfoxide (34 ml). To this mixture, a solution of potassium tert-butoxide (5.22 g, 46.55 mmol) in dimethyl sulfoxide (70 ml) was slowly added dropwise at 10° C., followed by stirring for 2 hours at 10° C. and for 15 hours at room temperature. Water was added to the reaction mixture, which was then extracted three times with ethyl acetate. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/9) to give 7-methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-one (1.78 g, Yield 79%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552068B1
Source datasetuspto-grants-2003_04
ORD IDord-5df879eace7e4b829809aad12e653c20
Source noteuspto-grants-2003_04