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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239248생성일: 2026년 10월 24일

Nitrogen → Methyl 3-amino-2-fluorobenzoate

https://huagongshe.com/ko/reaction/239248

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물ChloroformHCID 6212—
반응물Trifluoroacetic acidHCID 6422—
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl carbamateHCID 77922—
반응물Methyl 3-bromo-2-fluorobenzoateHCID 21584505—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Methyl 3-amino-2-fluorobenzoateHCID 4631108076.2%

반응 조건

온도90 °C

반응 단계

In a 500 mL flask was placed 1,1-dimethylethyl carbamate (6.03 g, 51.5 mmol), methyl 3-bromo-2-fluorobenzoate (10 g, 42.9 mmol), Pd2(dba)3.CHCl3 (0.89 g, 0.86 mmol), xantphos (1.49 g, 2.57 mmol) and cesium carbonate (16.8 g, 51.5 mmol). The flask was sealed with a rubber septum, placed under high vacuum, and toluene (200 mL) was added. Three cycles of high vacuum/N2 were performed and the reaction mixture was stirred at 90° C. overnight. The reaction was filtered through a pad of celite with EtOAc washing and concentrated. To the residue was added DCM (200 mL) followed by TFA (50 mL, 649 mmol), and the mixture was stirred at rt for 1 h. The volatiles were removed under reduced pressure and the residue was taken up in EtOAc and washed with saturated NaHCO3 and brine. The organic layer was dried over NaSO4, stripped onto silica and column chromatographed on silica with 5% to 50% EtOAc:Hexane to give 5.53 g (76%) of the title compound of Step B. 1H-NMR (400 MHz, DMSO-d6) δ 6.92-7.01 (m, 3H), 5.37 (s, 2H), and 3.81 (s, 3H). MS (ESI): 170 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642759B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d7c2abed2d7847de99c1a709d3358aa8
출처 메모uspto-grants-2014_02