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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639893Generated: October 26, 2026

Benzoyl chloride → N-(9-cyanobicyclo[3.3.1]non-9-yl)benzamide

https://huagongshe.com/reaction/1639893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium CarbonateHCID 11430—
ReactantWater methylene chlorideHCID 21908982—
Reactant9-Aminobicyclo[3.3.1]nonane-9-carbonitrileHCID 66720824—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(9-cyanobicyclo[3.3.1]non-9-yl)benzamideHCID 66721238—

Reaction Steps

Add a solution of 2.37 g (17.17 mmol) of potassium carbonate in 30 mL of water, then 1.37 mL (11.8 mmol) of benzoyl chloride, to a solution of 1.88 g (11.45 mmol) of 9-aminobicyclo[3.3.1]nonane-9-carbonitrile in 20 mL of THF. Stir the reaction mixture for 1 h at RT, then distribute in 100 mL of a 1:1 mixture of DCM/water. Wash the organic phase with 50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Solidify the residue obtained in 100 mL of pentane giving, after filtration and washing with pentane, 2.81 g of N-(9-cyanobicyclo[3.3.1]non-9-yl)benzamide in the form of white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110579B2
Source datasetuspto-grants-2012_02
ORD IDord-a024c2c213ec40e2adfc4a132caaa3d0
Source noteuspto-grants-2012_02