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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910483Generated: October 26, 2026

1,2-Dichloroethane → Bis(4-chlorophenyl)methyl quinuclidine-3-carboxylate

https://huagongshe.com/reaction/1910483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4,4'-DichlorobenzhydrolHCID 7033—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Azabicyclo(2.2.2)octane-3-carboxylic acid hydrochlorideHCID 12673436—
SolventTetrahydrofuranHCID 8028—
ProductBis(4-chlorophenyl)methyl quinuclidine-3-carboxylateHCID 7092582427.9%

Reaction Steps

Quinuclidine-3-carboxylic acid hydrochloride (150 mg, 0.78 mmol), EDC (225 mg, 1.17 mmol) and HOBT (180 mg, 1.17 mmol) were dissolved in dry THF (7.5 ml). Bis(4-chlorophenyl)methanol (218 mg, 0.86 mmol) was added followed by TEA (382 μl, 2.74 mmol). The resulting reaction was stirred at room temperature overnight. THF was removed under vacuum, and the crude was partitioned between EtOAc and water. The organic phase was washed with sat. NaHCO3, dried over sodium sulphate, filtered, and evaporated to dryness. The crude was purified by flash chromatography (EtOAc/MeOH=8/2 to 7:3+1% of NH4OH) to obtain bis(4-chlorophenyl)methyl quinuclidine-3-carboxylate (85.0 mg, racemic mixture).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-5946ae15d1684747a1fe17c1f788fb08
Source noteuspto-grants-2013_12