HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474482Generated: October 26, 2026
Acetic Anhydride → 4-((5-Methoxymethyl-2-furanyl)methylene)-2-(2-thienyl)-5(4H)-oxazolone
https://huagongshe.com/reaction/1474482
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-(Methoxymethyl)-2-furaldehyde | HCID 74711 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | ((2-Thienylcarbonyl)amino)acetic acid | HCID 679227 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-((5-Methoxymethyl-2-furanyl)methylene)-2-(2-thienyl)-5(4H)-oxazolone | HCID 75238472 | 50.7% |
Reaction Steps
To a screw-capped test tube, N-(2-thienylcarbonyl)glycine (56 mg, 0.3 mmol), 5-(methoxymethyl)-2-furancarboxaldehyde (46 mg, 0.3 mmol), sodium acetate (25 mg, 0.3 mmol) and acetic anhydride (0.3 mL) were added. The test tube was sealed, and it was then stirred at an external temperature of 90° C. Three hours later, the temperature of the reaction solution was returned to room temperature, and water (1.5 mL) was then added thereto. The obtained mixture was stirred at the same temperature as described above for 1.5 hours. Thereafter, the precipitated crystal was collected by filtration, and it was washed with water (5 mL) and was then dried under reduced pressure, so as to obtain 44 mg of the above-captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018238B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-78969d70748d4b8eb24d18508aa0bfd7 |
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| Source note | uspto-grants-2015_04 |
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