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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847283Generated: October 30, 2026

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

https://huagongshe.com/reaction/847283

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 numberUS05140046
Source datasetuspto-grants-1992_08
ORD IDord-5f149379a3b8410086e921a77f6fce17
Source noteuspto-grants-1992_08