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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301682Generated: October 30, 2026

Ethyl Acetate → HCID 11049546, compound

https://huagongshe.com/reaction/2301682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18345597HCID 18345597—
SolventTolueneHCID 1140—
ProductHCID 11049546HCID 1104954641.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

113 mg (0.176 mmols) of 6-chloro-9-[2-O-(sulfurylimidazolyl)-3-deoxy-5-O-(triphenylmethyl)-β-D-erythro-pentofuranosyl]-9H-purine was dissolved in 1.80 ml of toluene, to which was added 0.18 ml (1.06 mmols) of triethylamine trihydrofluoride, and stirred overnight at 50° C. After having been cooled, 10.0 ml of ethyl acetate and 8.0 ml of an aqueous saturated solution of sodium hydrogencarbonate were added to this, to separate it into layers. The organic layer was dried with anhydrous sodium sulfate, and filtered. Then, the solvent was evaporated from the filtrate. The residue was dissolved in acetonitrile and analyzed through liquid chromatography. The intended product was obtained at an yield of 41.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500946B1
Source datasetuspto-grants-2002_12
ORD IDord-76acda0900014925a5d01b6454a09bbf
Source noteuspto-grants-2002_12