Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910492Generated: November 2, 2026

2-Chloroacetophenone → HCID 70673624, compound

https://huagongshe.com/reaction/1910492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantHCID 70673880HCID 70673880—
SolventEthyl AcetateHCID 8857—
ProductHCID 70673624HCID 7067362468.3%

Reaction Steps

2-Chloro-1-phenylethanone (13 mg, 0.09 mmol) was added to a solution of (R)-bis(4-fluorophenyl)methyl quinuclidin-3-ylcarbamate (32.0 mg, 0.09 mmol, prepared as in example 3) in ethyl acetate (2 ml). The reaction was stirred at room temperature overnight. Then more 2-chloro-1-phenylethanone (2.7 mg, 0.02 mmol) was added to the solution, and the reaction was stirred for additional 24 hours. The reaction was evaporated to dryness, and the residue was triturated in Et2O. Then isopropyl ether was added, and the product was sonicated and the precipitate was collected by suction filtration to obtain (R)-3-((bis(4-fluorophenyl)methoxy)carbonylamino)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane chloride (32.4 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-4be59539d9c945208e5e1978860d9095
Source noteuspto-grants-2013_12