돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22182생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물6-Amino-2-methyl-3-nitrobenzoic acidHCID 15283172—
용매PyridineHCID 1049—
생성물6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-oneHCID 1528317379%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428021
출처 데이터셋uspto-grants-1995_06
ORD IDord-7a5418f062a74240945f6ad1b316d8b0
출처 메모uspto-grants-1995_06