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HRID 1375269作成日:2026年10月27日

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

https://huagongshe.com/reaction/1375269

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-BromotolueneHCID 7805—
反応物PentaneHCID 8003—
反応物6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
反応物HCID 178418306HCID 178418306—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2,2-Dimethyl-4(tol-4-yl)-6-bromo-thiochrom-3-eneHCID 86191487—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07166726B2
出典データセットuspto-grants-2007_01
ORD IDord-b10e5d2da0f245c48a4c83945586fbea
出典メモuspto-grants-2007_01