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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288307Generated: October 26, 2026

p-Toluenesulfonic acid → 2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-ene

https://huagongshe.com/reaction/2288307

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-BromotolueneHCID 7805—
ReactantPentaneHCID 8003—
Reactant6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
ReactantHCID 178418306HCID 178418306—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-eneHCID 86191487—

Reaction Steps

To a cold (-78° C.) solution of 4-bromotoluene (720 mg, 4.2 mmol) in THF (8 mL) was added t-BuLi in pentane (1.7M, 0.5 mL, 0.85 mmol). The mixture was warmed to ambient temperature over 30 minutes with stirring. This mixture was added to a flask containing 2,2-dimethyl-6-bromo-thiochroman-4-one (Compound M, 140 mg, 0.4 mmol) and THF (2 mL). and stirred for 16 hours at ambient temperature. The reaction was quenched by adding aq. NH4Cl, and the resulting mixture was extracted with ethylacetate, washed with brine, dried and the solvent was removed by evaporation. The product was isolated by chromatography on silica gel. The material was dissolved in dichloromethane (5 mL) and pTSA (5 mg) was added and heated to 50° C. for 3 hours. The misture was diluted with ethylacetate (20 mL), washed with 10% NaHCO3 (5 mL), brine (5 mL), dried with MgSO4 and the solvent was removed by evaporation to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087505
Source datasetuspto-grants-2000_07
ORD IDord-183e8195f1264d06b94218358075c62f
Source noteuspto-grants-2000_07