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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75835Generated: October 28, 2026

Tetrahydrofuran → HCID 67353855, compound

https://huagongshe.com/reaction/75835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 2-(3-(4-nitrophenyl)isoxazole-5-carboxamido)acrylateHCID 67355652—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67353855HCID 6735385518.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 2-(3-(4-nitrophenyl)isoxazole-5-carboxamido)acrylate (1.2 g, 3.78) was dissolved in EtOH (20 ml), THF (8 ml) and water (8 ml). Then ammonium chloride (601 mg, 11.34 mmol)) and iron (529 mg, 9.45) were added and refluxed at 80° C. for 1.5 hours. Reaction mixture was cooled and filtered through celite and solvent was removed under reduced pressure to get dark brown residue. Residue was taken in water and extracted with EtOAc. The organic layer was separated, dried over Na2SO4 and concentrated to get dark brown residue, which was purified by column chromatography using EtOAc and petroleum ether to yield 200 mg (18%) of the title compound. MS: ES (+): m/z 288 (M+1); 1HNMR (DMSO-d6, 300 MHz) δ: 10.115 (s, 1H), 7.577 (d, 2H), 7.558 (s, 1H), 6.640 (d, 2H), 6.011 (s, 1H), 5.873 (s, 1H), 5.642 (s, 2H), 3.753 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835428B2
Source datasetuspto-grants-2014_09
ORD IDord-f05c31a21ef64ca2bb9cee0f6b41103d
Source noteuspto-grants-2014_09