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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132242Generated: October 26, 2026

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

https://huagongshe.com/reaction/132242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,5-difluorobenzoic acidHCID 735965—
SolventTetrahydrofuranHCID 8028—
Product(2-Amino-4,5-difluorophenyl)methanolHCID 21925570—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384930B2
Source datasetuspto-grants-2008_06
ORD IDord-9efe20d592d94a859500b2c61ff42577
Source noteuspto-grants-2008_06