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HRID 2614생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2614

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-BromotolueneHCID 7805—
반응물PentaneHCID 8003—
반응물6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
반응물HCID 178418306HCID 178418306—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-eneHCID 86191487—

반응 단계

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 off.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728846
출처 데이터셋uspto-grants-1998_03
ORD IDord-1e1b81ee8df24843ab572b0af6fcff4f
출처 메모uspto-grants-1998_03