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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2288307Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2288307

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt4-BromotolueneHCID 7805—
EduktPentaneHCID 8003—
Edukt6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
EduktHCID 178418306HCID 178418306—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-eneHCID 86191487—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06087505
Quelldatensatzuspto-grants-2000_07
ORD IDord-183e8195f1264d06b94218358075c62f
Quellennotizuspto-grants-2000_07