HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486135Generated: October 29, 2026
Ethanimidic acid, ethyl ester, hydrochloride (1:1) → Methyl 5-(5-Methyl-1,3,4-oxadiazol-2-yl)-2-thiophenecarboxylate
https://huagongshe.com/reaction/486135
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanimidic acid, ethyl ester, hydrochloride (1:1) | HCID 2724290 | — |
| Reactant | 5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazide | HCID 14871961 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl 5-(5-Methyl-1,3,4-oxadiazol-2-yl)-2-thiophenecarboxylate | HCID 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 (C7H7O3S, 83%); 1HNMR (DMSO-d6) delta, 7.88 (1H, d, J=3.9Hz), 7.80 (1H, d, J=3.9Hz), 3.87 (3H, s), 2.58 (3H, s); ir (potassium bromide): 1705, 1571, 1291, 1101, 751 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05290802 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-73d40d64356a48949dac2819fffa5fdc |
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| Source note | uspto-grants-1994_03 |
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