HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520607Generated: October 28, 2026
Ethyl oxoacetate → Ethyl 1,3-oxazole-5-carboxylate
https://huagongshe.com/reaction/520607
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Toluenesulfonylmethyl isocyanide | HCID 53627694 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 1,3-oxazole-5-carboxylate | HCID 10964603 | — |
Reaction Steps
Toluenesulfonylmethyl isocyanide (TosMIc) (12.31 g, 1 wt, 1 eq) is dissolved in DCM (61.6 ml, 5 vols) at 0° C. under N2. In a separate vessel, ethyl glyoxalate (50 wt % solution in toluene, 20.6 g, 20.0 ml, 1.67 wt) is diluted with DCM (61.6 ml, 5 vols) under N2 and DBU (12.48 g, 12.35 ml, 1.3 eq, 1.01 wt) is added resulting in a purple solution. The second solution is added to the TosMIc solution over 1 hr, maintaining temperature at 0° C., then checked by HPLC for completion after a further 20 mins. The reaction is quenched by slow addition of 2M HCl (10 vols, 123 ml) and the DCM layer separated. The aqueous layer is re-extracted with DCM (5 vols, 61.6 ml), and the combined organics dried over Na2SO4, then evaporated on Buchi, 25° C., 100 mbar to remove DCM and toluene. Distilled at 12 mbar, jacket temperature 105° C., vapour temperature 60-80° C. to afford ethyl oxazole-5-carboxylate as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326987B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-86bdacb1a86a480c8d2bd9cb95c4a446 |
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| Source note | uspto-grants-2016_05 |
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