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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544588Generated: November 1, 2026

Benzoyl chloride → HCID 14367993, compound

https://huagongshe.com/reaction/544588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant3,7-Dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-olHCID 12360832—
SolventPyridineHCID 1049—
ProductHCID 14367993HCID 1436799342.5%

Reaction Steps

10 g of 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonane-9-ol are dissolved in 50 ml of dry pyridine, and a solution of 11.24 g of benzoyl chloride in 50 ml of dry pyridine is added dropwise, within 30 minutes, to the solution stirred at 5°-10° C. Thereafter the reaction mixture is stirred at room temperature for 3 hours, and the bulk of pyridine is distilled off under vacuo. The residue is taken up in 50 ml of water, the mixture is acidified with 20 ml of concentrated aqueous hydrochloric acid, and the mixture is extracted thrice with 50 ml of ether, each, in order to remove the non-basic substances. The aqueous phase is rendered alkaline with potassium carbonate and extracted thrice with 50 ml of chloroform, each. The chloroform solutions are combined, dried over magnesium sulfate, filtered, and the filtrate is evaporated. The residue is crystallized from n-hexane. 3,7-Dimethyl-9-benzoyloxy-3,7-diazabicyclo[3.3.1]nonane is obtained with a yield of 42.5%; m.p.: 100°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451473
Source datasetuspto-grants-1984_05
ORD IDord-530fece2ec3e4ebabbef8075edfa884c
Source noteuspto-grants-1984_05