HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877684Generated: October 31, 2026
Acetic Anhydride → Methyl 5-methyl-1,3-oxazole-4-carboxylate
https://huagongshe.com/reaction/1877684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-methyl-1,3-oxazole-4-carboxylate | HCID 12627321 | — |
Reaction Steps
A stirred mixture of methyl isocyanoacetate (7.0 g, 70 mmol, 1 eq) and DBU (10.06 g, 70 mmol, 1 eq) in THF was cooled to 0° C., and a solution of acetic anhydride (7.14 g, 70 mmol, 1 eq) in THF was added dropwise over 15 min. The reaction mixture was stirred for 12 h at room temperature. The solvent was removed by Rota-vapor and water was added. The mixture was extracted with EtOAc. The crude product was purified by silica gel (230-400) column chromatography using 30% EtOAc/hexane. Yield: 6.8 g (98%). 1H NMR (400 MHz, CDCl3): δ 2.54 (s, 3H), 3.80 (s, 3H), 7.69 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309558B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-622144812ca7472b99bf254c6eecd3cc |
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| Source note | uspto-grants-2012_11 |
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