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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619570Generated: November 3, 2026

Benzoyl chloride → (R)-quinuclidin-3-yl 2-benzamido-2-(4-chlorophenyl)acetate

https://huagongshe.com/reaction/1619570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant(R)-quinuclidin-3-yl 2-amino-2-(4-chlorophenyl)acetate dihydrochlorideHCID 67606496—
SolventDichloromethaneHCID 6344—
Product(R)-quinuclidin-3-yl 2-benzamido-2-(4-chlorophenyl)acetateHCID 6760748498.7%

Reaction Steps

To a suspension of (R)-quinuclidin-3-yl 2-amino-2-(4-chlorophenyl)acetate dihydrochloride (I112) (0.12 g, 0.32 mmol) in DCM (5 ml), were added triethylamine (0.13 ml, 0.95 mmol) and benzoyl chloride (44.0 μl, 0.38 mmol), and the reaction was stirred at RT for 3 hours. Then the solvent was evaporated, and the residue was taken up with EtOAc and washed with Na2CO3, water and brine. The organic layer was dried over Na2SO4, filtered and evaporated to obtain (R)-quinuclidin-3-yl 2-benzamido-2-(4-chlorophenyl)acetate (0.126 g; quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772314B2
Source datasetuspto-grants-2014_07
ORD IDord-f7369056c8df4cd88267a66feadeb14d
Source noteuspto-grants-2014_07