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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1399419생성일: 2026년 10월 27일

Triethylamine → 2,4-Dinitrobenzoyl chloride

https://huagongshe.com/reaction/1399419

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4-Dinitrobenzoic acidHCID 11880—
반응물Thionyl ChlorideHCID 24386—
생성물2,4-Dinitrobenzoyl chlorideHCID 88401—
생성물Benzyl glycinateHCID 409140—

반응 단계

As shown in scheme B, treatment of 2,4-dinitrobenzoic acid with chlorinating agent such as thionyl chloride gave 2,4-dinitrobenzoyl chloride which on further treatment with benzyl glycinate in the presence of triethylamine gave benzyl 2-(2,4-dinitrobenzamido)acetate (intermediate 1). The intermediate 1 is treated either with K18F or K19F in the presence of a catalyst such as kryptofix[2.2.2] or 18-crown-6 to yield benzyl 2-(2-fluoro-4-nitrobenzamido)acetate, which on reduction with hydrogen gas or hydrogen source in the presence of Pd/C gave 2-(4-amino-2-fluorobenzamido)acetic acid (compound 1) in good yield. Alternatively, treatment of 2,4-dinitrobenzoyl chloride with glycine in presence of a mild base such as sodium carbonate gave 2-(2,4-dinitrobenzamido)acetic acid (intermediate 2). Treatment of intermediate 2 either with K18F or K19F gave 2-(2-fluoro-4-nitrobenzamido)acetic acid, which on reduction with zinc dust and ammonium formate or hydrogen gas/hydrogen source in the presence of Pd/C gave compound 1. Treatment of intermediate 2 either with K18F or K19F and further reduction with iron powder in the presence of acetic anhydride-acetic acid gave 2-(4-acetamido-2-fluorobenzamido)acetic acid (compound 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08906344B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-019a024964ef422eb47b448b4d5e4f65
출처 메모uspto-grants-2014_12