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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910491Generated: October 30, 2026

2-Chloroacetophenone → HCID 86672926, compound

https://huagongshe.com/reaction/1910491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantHCID 70675260HCID 70675260—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672926HCID 8667292674.7%

Reaction Steps

2-Chloro-1-phenylethanone (55.0 mg, 0.36 mmol) was added to a solution of (R)-benzhydryl quinuclidin-3-ylcarbamate (100 mg, 0.30 mmol, prepared as in example 2) in ethyl acetate (4 ml). The reaction was stirred at room temperature overnight. The suspension was decanted, solvent was removed, and the product was evaporated to dryness. Et2O was added, and the suspension was sonicated. The precipitate was collected by suction filtration and dried under vacuum at 40° C. to obtain (R)-3-(benzhydryloxycarbonylamino)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo-[2.2.2]octane chloride (110 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-d279ad35cff04b23be75e4d50191fda1
Source noteuspto-grants-2013_12