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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625990Generated: November 3, 2026

Ammonium Chloride → HCID 87260512, compound

https://huagongshe.com/reaction/1625990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantEthyl tetrahydropyran-4-ylacetateHCID 2773412—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87260512HCID 87260512—

Reaction Steps

Ethyl 2-(tetrahydro-2H-pyran-4-yl)acetate (2.0 g) was dissolved in tetrahydrofuran (20 ml). A solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran (1.0 M, 17 ml) was added dropwise under nitrogen atmosphere under ice-cooling, and the mixture was stirred at the same temperature for 15 minutes. Then, a solution of N-fluorobenzenesulfonimide (7.3 g) in tetrahydrofuran (20 ml) was added and the mixture was stirred at the same temperature for 3 hours. A saturated aqueous ammonium chloride solution and water were added under ice-cooling, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated. Chloroform-diethyl ether was added to the residue, and insoluble matter was removed by filtration. Thereafter, the solvent was evaporated and the residue was purified by silica gel column chromatography (developed with ethyl acetate-hexane and with chloroform) to give the title compound containing insoluble matter (0.9 g) as a pale orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785438B2
Source datasetuspto-grants-2014_07
ORD IDord-59059a9dca714fb588199b3781345aea
Source noteuspto-grants-2014_07