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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619568Generated: November 3, 2026

Benzoyl chloride → HCID 67606235, compound

https://huagongshe.com/reaction/1619568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 67607082HCID 67607082—
SolventDichloromethaneHCID 6344—
ProductHCID 67606235HCID 6760623556%

Reaction Steps

To a suspension of (R)-quinuclidin-3-yl 2-amino-2-p-tolylacetate dihydrochloride (I109) (116 mg, 0.33 mmol) in DCM (5 ml), were added triethylamine (139 μl, 1.00 mmol) and benzoyl chloride (46.5 μl, 0.40 mmol). The reaction was stirred at RT for 3 hours, and then the solvent was evaporated. The residue was taken up with EtOAc and washed with Na2CO3, water and brine. The organic phase was dried over Na2SO4, filtered and evaporated to obtain (R)-quinuclidin-3-yl 2-benzamido-2-p-tolylacetate (70.0 mg; 55% yield). The product was used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772314B2
Source datasetuspto-grants-2014_07
ORD IDord-90564dfa511a409a85582daeca368ce1
Source noteuspto-grants-2014_07