HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22186Generated: October 29, 2026
Ethyl chloroformate → HCID 15283178, compound
https://huagongshe.com/reaction/22186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 15283177 | HCID 15283177 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 15283178 | HCID 15283178 | 47% |
Reaction Steps
A solution of 1.3 g (6.2 mmoles) of 5-nitro-6-ethyl-2-aminobenzoic acid in 40 mL of dry pyridine was cooled in an ice-water bath under inert atmosphere. Ethyl chloroformate, 2 mL (21 mmoles), was added dropwise over a five-minute period. A mild exotherm was observed and a solid separated from solution immediately upon addition. The suspension was stirred in the ice-water bath for 60 minutes, then warmed to room temperature and stirred under inert atmosphere overnight. Approximately half the pyridine was removed in vacuo, and the residual mixture was poured over ice. The precipitated solid, an orange brown color, was collected and air-dried. 0.76 g (47% yield) 6-nitro-5-ethyl-2-ethoxy-3,1-benzoxazin-4-one was obtained. NMR(CDCl3): 1.36(t,3H,J=7.5 Hz), 1.47(t,3H,J=7.2 Hz), 3.27(q,2H,J=7.2 Hz), 4.56(q,2H, J=7.5 Hz), 7.36(d,1H,J=9.0 Hz), 7.98(d,1H,J=9.0 Hz). MS(m/z): 282(M+ +H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428021 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-eb8c7309f6234b9f9292ddc9ac5f6203 |
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| Source note | uspto-grants-1995_06 |
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