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HRID 217315作成日:2026年10月27日

Ammonium Chloride → Tetralin

https://huagongshe.com/reaction/217315

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Bis(pyridine)iodonium tetrafluoroborateHCID 10883201—
反応物1-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-buteneHCID 25111988—
溶媒DichloromethaneHCID 6344—
生成物TetralinHCID 840471%

反応条件

温度-78 °C

反応手順

Bis(pyridine)iodonium tetrafluoroborate (65.8 mg, 0.177 mmol) was suspended in methylene chloride (3.4 mL), and the suspension was cooled to −78° C. in a dry ice/acetone bath. A methylene chloride (1.8 mL) solution of 1-(4-methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-butene (4, 56.0 mg, 0.135 mmol) was added to the suspension, and also a tribromoborane diethyl ether complex (0.015 mL, 0.118 mmol) was added stepwise three times. Thereafter, the reactant was stirred at −78° C. for 1 hour, then a saturated aqueous ammonium chloride solution (5 mL) was added thereto to stop the reaction, and the reactant was cooled to room temperature and then extracted three times with diethyl ether (10 mL). An organic layer was collected and rinsed with a saturated aqueous sodium chloride solution (10 mL), followed by drying with anhydrous sodium sulfate and concentrating. The residue was purified by thin layer chromatography to obtain the title compound as a light yellow oily substance (51.6 mg, yield 71%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193394B2
出典データセットuspto-grants-2012_06
ORD IDord-db6a93e85f2b487fb201bf56678cdfe7
出典メモuspto-grants-2012_06