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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706600Generated: November 1, 2026

Pyridine → HCID 3402305, compound

https://huagongshe.com/reaction/1706600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPyrrolidineHCID 31268—
Reactant2-Phenoxybenzoyl chlorideHCID 11075303—
SolventWaterHCID 962—
ProductHCID 3402305HCID 3402305—

Reaction Steps

7.7 parts of 2-phenoxybenzoyl chloride was added dropwise to a solution of 2.5 parts of pyrrolidine in 20 parts of pyridine at 0°. When the addition was complete the mixture was stirred for 5 hours. The temperature was then allowed to rise to room temperature and the reaction mixture was poured into 100 parts of water. The aqueous solution was then extracted with chloroform, and washed with water. The chloroform layer was dried over magnesium sulfate, removal of the magnesium sulfate by filtration and concentration of the filtrate gave 6.4 parts of N-(2-phenoxybenzoyl)pyrrolidine, NMR (CDCl3) 1.8δ(m,4H,CH2), 3.4δ(m,4H-N-CH2), 7.1δ(m,9H,Aromatic H). The following compounds can be prepared from the 2-substituted benzoyl chloride and the appropriate secondary amine as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208205
Source datasetuspto-grants-1980_06
ORD IDord-02e3141ad9d74baead51f93f9cf6ccb0
Source noteuspto-grants-1980_06