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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22186Generated: October 29, 2026

Ethyl chloroformate → HCID 15283178, compound

https://huagongshe.com/reaction/22186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 15283177HCID 15283177—
SolventPyridineHCID 1049—
ProductHCID 15283178HCID 1528317847%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428021
Source datasetuspto-grants-1995_06
ORD IDord-eb8c7309f6234b9f9292ddc9ac5f6203
Source noteuspto-grants-1995_06