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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132378생성일: 2026년 10월 26일

2-Amino-4,5-difluorobenzoic acid → (2-Amino-4,5-difluorophenyl)methanol

https://huagongshe.com/reaction/132378

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4,5-difluorobenzoic acidHCID 735965—
용매TetrahydrofuranHCID 8028—
생성물(2-Amino-4,5-difluorophenyl)methanolHCID 21925570—

반응 단계

2-Amino-4,5-difluorobenzoic acid (5.37 g, 31.0 mmol) in THF (50 mL) was dropwise added to the suspension on LAH (1.65 g, 43.5 mmol) in THF (15 mL) at room temperature under N2 over 10 min. The resulting suspension was stirred at room temperature for 1 hr. Then the mixture was cooled down to 0° C., quenched with saturated Na2SO4 (100 mL), and extracted with Et2O (2×100 mL), the combined organic layers were washed with brine (60 mL), dried over MgSO4, and concentrated on rotary vacuum to afford the expected crude product as a brown solid, which was pure enough to be used in next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 4.07 (s, 1 H), 4.56 (s, 2 H), 6.46 (dd, J=11.71, 6.92 Hz, 1 H), 6.87 (dd, J=10.58, 8.56 Hz, 1 H); Mass spec. 160.04 (MH+), Calc. for C7H7F2NO 159.05.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384931B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-2b1c29c9560b40549636e0c448a68fd2
출처 메모uspto-grants-2008_06