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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581077Generated: October 27, 2026

Ethanimidic acid, ethyl ester, hydrochloride (1:1) → Methyl 5-(5-Methyl-1,3,4-oxadiazol-2-yl)-2-thiophenecarboxylate

https://huagongshe.com/reaction/581077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
Reactant5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazideHCID 14871961—
SolventPyridineHCID 1049—
ProductMethyl 5-(5-Methyl-1,3,4-oxadiazol-2-yl)-2-thiophenecarboxylateHCID 14871962—

Reaction Steps

A stirred suspension of 5-methoxycarbonyl-2-thiophenecarboxylic acid hydrazide (548 mg, 2.74 mmoles) and ethyl acetimidate hydrochloride (372 mg, 3.01 mmoles) in 10 ml of pyridine was refluxed for four hours, cooled to room temperature and evaporated in vacuo. The residual oily solid was dissolved in ethyl acetate and washed with water, 1N hydrochloric acid and 5% sodium bicarbonate. The ethyl acetate was dried magnesium sulfate) and evaporated in vacuo to a pale tan solid (242 mg, 39%), m.p. 142-5° C. This material was used directly without further purification. Exact Mass: 224.0253, Calculated: 224.0256; EIMS (m/z): 224 (M+, base), 193 (M+ --CH3O, 33%), 169 (C7H5O3S, 83%); 1HNMR (DMSO-d6) delta, 7.88 (1H, d, J=3.9 Hz), 7.80 (1H, d, J=3.9 Hz), 3.87 (3H, s), 2.58 (3H, s); ir (potassium bromide): 1705, 1571, 1291, 1101, 751 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919809
Source datasetuspto-grants-1999_07
ORD IDord-1ffa8dd208e44773a373496e818c9f26
Source noteuspto-grants-1999_07