Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386622Generated: November 1, 2026

Dimethylformamide → 2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazole

https://huagongshe.com/reaction/1386622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(Hexyloxy)benzoic acidHCID 70834—
ReactantBenzoyl chloride, 4-(hexyloxy)-HCID 170235—
ReactantEthyl 3-amino-4-hydroxybenzoateHCID 12208891—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
SolventOxalyl chlorideHCID 65578—
Product2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazoleHCID 21182488—

Reaction Steps

To a suspension of 4-hexyloxybenzoic acid in oxalyl chloride (10 ml) and dichloromethane (10 ml) was added N,N-dimethylformamide (0.1 ml). The mixture was stirred at room temperature for 2 hours. The solvent was removed under reduced pressure to give crude 4-hexyloxybenzoate chloride. To a suspension of Ethyl 3-amino-4-hydroxybenzoate (733 mg) and triethylamine (1.38 ml) and 4-dimethylaminopyridine (DMAP, 10 mg) in methylene chloride (10 ml) was added the solution of 4-hexyloxybenzoyl chloride obtained above in dichloromethane (5 ml) dropwise at 10° C. The reaction mixture was stirred at 10° C. for 1.5 hours and diluted with dichloromethane (20 ml). the solution was washed with H2O (20 ml), 1N HCl aq. (20 ml×2), H2O (20 ml) and brine (20 ml) successively. The organic layer was dried over MgSO4 and the solvent was removed under reduced pressure. To the residue was added toluene (15 ml) and p-toluenesulfonic acid (10 mg). The mixture was refluxed for 6 hours and the solvent was removed under reduced pressure. The residue was triturated with acetonitrile, and precipitate was collected with filtration and dried over PO5 to give 2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazole (0.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265536B1
Source datasetuspto-grants-2001_07
ORD IDord-506352229fd7463aaa47c7ab5d4662d6
Source noteuspto-grants-2001_07