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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112385Generated: October 25, 2026

Triethylamine → 2-(4-Chlorobutyramido)-4-methyloxazole

https://huagongshe.com/reaction/1112385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant4-Methyloxazol-2-amineHCID 535824—
SolventBenzeneHCID 241—
Product2-(4-Chlorobutyramido)-4-methyloxazoleHCID 2132364523.92%

Reaction Steps

2-Amino-4-methyloxazole (5.0 g., 0.0509 mol) was dissolved in dry benzene (100 mls.) and triethylamine (5.70 g., 0.0563 mol) was added. The mixture was stirred vigorously at room temperature and 4-chlorobutyrylchloride (7.88 g., 0.0558 mol) in dry benzene (50 mls.) was added rapidly. After the addition the mixture was heated under reflux for 2 hours. The mixture was then cooled and fltered. The filtrate was placed in a separating funnel and washed successively with water (1 × 100 mls.), 10% Na2CO3 (2 × 100 mls.) and water (3 × 100 mls.). The organic layer was driec over magnesium sulphate and evaporated under vacuum. The product was recrystallised from ethyl acetate/hexane. Wt. = 2.47 g. m.p. 98° C. (Yield = 23.92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04122183
Source datasetuspto-grants-1978_10
ORD IDord-35832c43f16d46d1ab02c407a8a7d7eb
Source noteuspto-grants-1978_10