Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483593Generated: October 30, 2026

Pyridine → HCID 10072632, compound

https://huagongshe.com/reaction/483593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Aminobenzyl alcoholHCID 80293—
Reactantp-TetradecyloxyphenylacetylchlorideHCID 10021844—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10072632HCID 1007263277%

Reaction Steps

To a solution of 15.5 g of m-aminobenzyl alcohol and 36.21 g of pyridine in 250 ml of tetrahydrofuran, cooled to 0° C. is added over 40 minutes a solution of 42 g of p-tetradecyloxyphenylacetyl chloride in 250 ml of tetrahydrofuran. The mixture is stirred overnight at room temperature and the solvent is evaporated. The residue is partitioned between water and chloroform with some heating to afford a complete solution. The hot chloroform solution is washed with warm water and warm dilute hydrochloric acid. The organic layer is dried and evaporated to a residue which is crystallized from carbon tetrachloride to give 40 g of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225425
Source datasetuspto-grants-1993_07
ORD IDord-add5ed77324d4c239091ad87f5096867
Source noteuspto-grants-1993_07