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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197092Generated: October 31, 2026

Oxalyl chloride → Ethyl 6-[o-[p-(4-phenylbutoxy)benzamido]phenyl]hexanate

https://huagongshe.com/reaction/1197092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-(4-Phenylbutoxy)benzoic AcidHCID 11043825—
ReactantBenzoyl chloride, 4-(4-phenylbutoxy)-HCID 11055348—
ReactantEthyl 6-(o-aminophenyl)hexanateHCID 19882678—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-[o-[p-(4-phenylbutoxy)benzamido]phenyl]hexanateHCID 19882682—

Reaction Steps

A solution of p-(4-phenylbutoxy)benzoyl chloride prepared from 1 g of p-(phenylbutoxy)benzoic acid and 2 ml of oxalyl chloride in methylene chloride was added to a solution of 0.6 g of ethyl 6-(o-aminophenyl)hexanate obtained in Reference Example 17 in 10 ml of pyridine at temperature less than -30° C. The mixture was stirred at room temperature overnight and concentrated under reduced pressure. Toluene was added to the residue. The mixture was washed with diluted hydrochloric acid and then with water and dried over anhydrous magnesium sulfate. The systems was concentrated under reduced pressure to obtain 1.0 g of oily ethyl 6-[o-[p-(4-phenylbutoxy)benzamido]phenyl]-hexanate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116853
Source datasetuspto-grants-1992_05
ORD IDord-bc855de65d1a4d9fa5c4303a1573a0fb
Source noteuspto-grants-1992_05