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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859337Generated: October 30, 2026

Potassium Carbonate → 7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-one

https://huagongshe.com/reaction/1859337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 10969180HCID 10969180—
SolventAcetonitrileHCID 6342—
Product7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-oneHCID 11130368—

Reaction Conditions

Temperature60 °C

Reaction Steps

To acetonitrile solution (120 ml) of 2-(4-methoxyphenyl)-3-(3-methoxyphenylthio)propionic acid (4) (12.8 g, 40.3 mmol) obtained above was added potassium carbonate (1.59 g, 11.5 mmol) and phosphorus oxychloride (18.7 ml, 200 mmol) at 0° C. and then stirred for 18 hours at 60° C. The reaction solution was quenched with ice-water and extracted with ether. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and then distilled under reduced pressure to remove the solvent. The obtained crude product was washed with ether to obtain 6.8 g of the first crop of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (5). Further, the filtrate was concentrated and the residue was then purified with silica gel column chromatography (ethyl acetate:hexane=1:3) to obtain 1.0 g of the second crop of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (5) (total yield: 7.8 g, 65%). NMR data of the compound (5) was identical to that described in Example 25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153768
Source datasetuspto-grants-2000_11
ORD IDord-0ad73b2939144917845e6748e62f173b
Source noteuspto-grants-2000_11