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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217315Generated: October 25, 2026

Ammonium Chloride → Tetralin

https://huagongshe.com/reaction/217315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBis(pyridine)iodonium tetrafluoroborateHCID 10883201—
Reactant1-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-buteneHCID 25111988—
SolventDichloromethaneHCID 6344—
ProductTetralinHCID 840471%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193394B2
Source datasetuspto-grants-2012_06
ORD IDord-db6a93e85f2b487fb201bf56678cdfe7
Source noteuspto-grants-2012_06