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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088955Generated: November 1, 2026

Ammonium Chloride → HCID 87260512, compound

https://huagongshe.com/reaction/2088955

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 numberUS08436012B2
Source datasetuspto-grants-2013_05
ORD IDord-4c266270683e4ecca897fe783fb8a2bc
Source noteuspto-grants-2013_05