Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780893Generated: October 31, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyloxazole-4-carboxamide

https://huagongshe.com/reaction/1780893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCl dichloromethaneHCID 19696284—
ReactantMethyl oxazole-4-carboxylateHCID 22647202—
Solvent1,1-DichloroethaneHCID 6365—
ProductN-Methoxy-N-methyloxazole-4-carboxamideHCID 4508444881.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methoxy-methylamine hydrochloride (2.3 g, 23.6 mmol) in 30 mL of dichloroethane at 0° C. was added dropwise 11.8 mL (23.6 mmol) of trimethylaluminum. The mixture was stirred at 0° C. for 20 min, and methyl 4-oxazolecarboxylate (1 g, 7.9 mmol) in 20 mL of dichloroethane was added in one portion. The mixture was poured into an ice-cold solution of 0.5 N HCl/methylene chloride (2:1) and stirred for 10 min. The aqueous layer was extracted with methylene chloride (2×50 mL), and the combined organic layer was washed with saturated ammonium chloride solution, dried over sodium sulfate, and concentrated in vacuo. The resulting residue was purified by chromatography on silica (methylene chloride/ethyl acetate/methanol 6:3:1) to afford 1.0 g (81.9%) of 4-oxazolyl-N-methyl-N-methoxy-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631264
Source datasetuspto-grants-1997_05
ORD IDord-014a007eaa59417cac0e36c00e86ebde
Source noteuspto-grants-1997_05