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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463484Generated: November 1, 2026

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

https://huagongshe.com/reaction/1463484

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 (M30 --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 numberUS05300655
Source datasetuspto-grants-1994_04
ORD IDord-6d63a2c2a1374d81a0184ff00f5f122f
Source noteuspto-grants-1994_04