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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397239Generated: October 26, 2026

Methyl 5-((hydroxyimino)methyl)thiophene-2-carboxylate → HCID 14871948, compound

https://huagongshe.com/reaction/1397239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-((hydroxyimino)methyl)thiophene-2-carboxylateHCID 72740488—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 14871948HCID 1487194899.7%

Reaction Steps

A solution of methyl 5-((hydroxyimino)methyl)thiophene-2-carboxylate (440 mg, 2.4 mmol) in acetic anhydride (10 mL) was refluxed for 16 h. After completion, the reaction mixture was cooled to room temperature, concentrated under reduced pressure and the residue was dissolved in diethyl ether. The organic layer was washed with 10% aqueous NaOH solution, water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to yield methyl 5-cyanothiophene-2-carboxylate (5-cyano-thiophene-2-carboxylic acid methyl ester) (400 mg, yield 90%) which was carried through without any further purification. 1H NMR (400 MHz, DMSO-d6) δ 7.77 (d, J=4.2 Hz, 1H), 7.60 (d, J=4.1 Hz, 1H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-a5fb5d6652714366a689781b8c78d6d9
Source noteuspto-grants-2014_12