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HRID 132378作成日:2026年10月27日

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

https://huagongshe.com/reaction/132378

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4,5-difluorobenzoic acidHCID 735965—
溶媒TetrahydrofuranHCID 8028—
生成物(2-Amino-4,5-difluorophenyl)methanolHCID 21925570—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384931B2
出典データセットuspto-grants-2008_06
ORD IDord-2b1c29c9560b40549636e0c448a68fd2
出典メモuspto-grants-2008_06