Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872782Generated: October 25, 2026

Triethylamine → Ethyl 5-[(morpholin-4-yl)methyl]-1,2-oxazole-3-carboxylate

https://huagongshe.com/reaction/872782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(2-Propyn-1-yl)morpholineHCID 412941—
ReactantEthyl 2-chloro-2-(hydroxyimino)acetateHCID 6399471—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 5-[(morpholin-4-yl)methyl]-1,2-oxazole-3-carboxylateHCID 23006302—

Reaction Steps

To the solution of ethyl chlorooximidoacetate (0.588 g, 3.88 mmol) and 4-(prop-2-ynyl)morpholine (0.971 g, 7.76 mmol) in toluene (5 mL) was added solution of triethylamine (0.54 mL, 3.88 mmol) in toluene (5 mL) dropwise. The resultant mixture was stirred at RT for 5 h. After the completion of the reaction as evidenced by LC-MS, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic solvent was then dried over anhydrous sodium sulfate and evaporated. The crude product was purified by Combiflash (Heptane:EtOAc eluent). Yield 0.2 g. 1H NMR (400 MHz; MeOD): δ 1.38 (t, 3H), 2.53 (m, 4H), 3.69 (m, 4H), 3.78 (d, 2H), 4.41 (q, 2H), 6.73 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-7308ad297900412db1a4865e1737e70c
Source noteuspto-grants-2015_03