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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910511Generated: October 27, 2026

1,2-Dichloroethane → (3,4-Difluorophenyl)(phenyl)methyl quinuclidine-3-carboxylate

https://huagongshe.com/reaction/1910511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(3,4-Difluorophenyl)(phenyl)methanolHCID 2758251—
Reactant1-Azabicyclo(2.2.2)octane-3-carboxylic acid hydrochlorideHCID 12673436—
SolventTetrahydrofuranHCID 8028—
Product(3,4-Difluorophenyl)(phenyl)methyl quinuclidine-3-carboxylateHCID 7092585543.3%

Reaction Steps

Quinuclidine-3-carboxylic acid hydrochloride (80 mg, 0.42 mmol), EDC (120 mg, 0.62 mmol), and HOBT (96 mg, 0.62 mmol) were dissolved in dry THF (3 ml). (3,4-Difluorophenyl)(phenyl)methanol (101 mg, 0.46 mmol) was dissolved in dry THF (2 ml) and then added to the reaction mixture. Triethylamine (203 μl, 1.46 mmol) was finally added, and the resulting reaction was stirred at room temperature overnight. The volatiles were evaporated, and the crude was taken up with EtOAc and washed with water and then with sat. NaHCO3. The organic phase was dried over sodium sulfate, filtered, and evaporated under vacuum. The crude was purified by flash chromatography (DCM/MeOH=9/1) to obtain (3,4-difluorophenyl)(phenyl)-methyl quinuclidine-3-carboxylate (65 mg, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-c0f7c0dcb0224b5ca311e8403c7d6e60
Source noteuspto-grants-2013_12