HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817300Generated: October 27, 2026
Chloroform → Ethyl 5-butoxy-1,3-oxazole-2-carboxylate
https://huagongshe.com/reaction/1817300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | butyl N-[ethoxy(oxo)acetyl]glycinate | HCID 69643286 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Ethyl 5-butoxy-1,3-oxazole-2-carboxylate | HCID 66996945 | — |
Reaction Steps
A suspension of P2O5 (22 g, 155.6 mmol) in CH3CN (50 mL) under nitrogen was warmed to 50° C. and treated with butyl N-[ethoxy(oxo)acetyl]glycinate (6 g, 25.9 mmol) dissolved in 10 mL CH3CN. The mixture was heated to 65° C. for 1.5 hours, then cooled in an ice bath. Ice and brine were added to the reaction mixture, then EtOAc was added and the mixture transferred to a separatory funnel. CHCl3 was added to dissolve solids and the organic layer was isolated. The aqueous layer was washed repeatedly with CHCl3 and EtOAc, the organic layers were combined and dried with Na2SO4, then concentrated. The residue was chromatographed on silica eluting with a gradient of 0-30% EtOAc/Hexanes to give the product as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598264B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-f2dc169bf52842899053df8afcd8fa41 |
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| Source note | uspto-grants-2009_10 |
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