Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119050Generated: October 25, 2026

Triethylamine → 4,5-Dihydro-5-(3-hydroxyphenyl)-2-(2-thienyl)-1,3-oxazole

https://huagongshe.com/reaction/2119050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzenemethanol, alpha-(aminomethyl)-3-hydroxy-, hydrochloride (1:1)HCID 3016408—
ReactantEthyl thiophene-2-carboximidate hydrochlorideHCID 12231044—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4,5-Dihydro-5-(3-hydroxyphenyl)-2-(2-thienyl)-1,3-oxazoleHCID 1392137081.5%

Reaction Steps

A mixture of (±) norphenylephrine hydrochloride (10 g, 0.05 mol), ethyl thiophene-2-imidate hydrochloride (10 g, 0.05 mol) and triethylamine (5 g, 0.05 mol) in tetrahydrofuran (300 ml) is heated to reflux for 8 hours. The mixture is dissolved in ethyl acetate and water. The aqueous layer is extracted twice with ethyl acetate. The combined ethyl acetate solutions are washed twice with dilute aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated to dryness to obtain a viscous, partly crystalline material (10 g). This material is triturated with ether to obtain crystals (5 g) of m.p. 150°. These crystals are dissolved in hot acetonitrile and the solution is filtered and allowed to cool. The crystals (3.4 g) are filtered off, washed with acetonitrile and dried in vacuo; m.p. 156°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04681940
Source datasetuspto-grants-1987_07
ORD IDord-c34648ca46254b91984891f318c9e8a7
Source noteuspto-grants-1987_07