Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132775Generated: October 31, 2026

Pyridine → HCID 69199532, compound

https://huagongshe.com/reaction/132775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 69198279HCID 69198279—
SolventDichloromethaneHCID 6344—
ProductHCID 69199532HCID 69199532—

Reaction Steps

5.24 grams of 2-p-methylbenzyl-2-ethoxycarbonyl-cyclopentanol obtained in Example 18 were diluted with 60 ml of methylene chloride. At room temperature and with magnetic stirring, 2.44 ml of pyridine was slowly added, then 3.55 ml of benzoyl chloride was dropwise added. Upon the completion of the addition, the reaction was continued under reflux condition for 12 hours. Then the procedure as described in Example 23 was followed, to give 7.41 g of yellow liquid. MS: m/e 367(M++1), 366(M+), 293(M+—CO2CH2CH3), 261(M+—C6H5CO2), 216, 198, 170, 155, 105, 91, 77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388103B2
Source datasetuspto-grants-2008_06
ORD IDord-1beffa53294b4b3dba14c49c73b25854
Source noteuspto-grants-2008_06