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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22182Generated: October 23, 2026

Ethyl chloroformate → 6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one

https://huagongshe.com/en/reaction/22182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant6-Amino-2-methyl-3-nitrobenzoic acidHCID 15283172—
SolventPyridineHCID 1049—
Product6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-oneHCID 1528317379%

Reaction Steps

A solution of 4.0 g (20.4 mmoles) of 5-nitro-6-methyl-2-aminobenzoic acid in 50 mL of dry pyridine was cooled in an ice-water bath under inert atmosphere. Ethyl chloroformate (Aldrich), 10 mL (105 mmoles), was added dropwise over a 15 minute period. A mild exotherm was observed and a solid separated from solution immediately upon addition. The suspension was stirred at room temperature under inert atmosphere overnight. Approximately half the pyridine was removed in vacuo, and the residual mixture poured over ice. The precipitated solid was collected and air-dried. 4.0 g (79% yield) 6-nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one was obtained. NMR (DMSO-d6): 1.37(t,3H,J=7.2 Hz), 2.71(s,3H), 4.50(q,2H,J=7.2 Hz), 7.40(d,1H, J=9.0 Hz), 8.19(d,1H,J=9.0 Hz). IR(nujol): 1765 cm-1 (lactone carbonyl). MS(m/z): 250(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428021
Source datasetuspto-grants-1995_06
ORD IDord-7a5418f062a74240945f6ad1b316d8b0
Source noteuspto-grants-1995_06