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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38682Generated: October 28, 2026

Aluminium lithium hydride → (3-Amino-2-fluorophenyl)methanol

https://huagongshe.com/reaction/38682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-Amino-2-fluorobenzoic acidHCID 23094343—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(3-Amino-2-fluorophenyl)methanolHCID 5324922950.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-amino-2-fluorobenzoic acid (APIN, 250 mg, 1.612 mmol) was dissolved in 10 mL of anhydrous THF under N2 atmosphere. Solution was cooled at 0° C. in an ice-water bath. LiAlH4 (FLUKA, 183 mg, 4.83 mmol) was added. Reaction was stirred under nitrogen at room temperature. After 2 h one equivalent of LiAlH4 (FLUKA, 61 mg, 1.62 mmol) was added to the mixture and reaction was stirred at room temperature overnight. Another equivalent of LiAlH4 (FLUKA, 61 mg, 1.62 mmol) was added. After 5 h The reaction mixture was quenched by adding MeOH. Solvent was evaporated to obtain an orange syrup that was dissolved in EtOAc and partitioned with saturated NaHCO3 (aqueous) (10 mL of saturated solution+15 mL of distilled water). Aqueous phase was extracted with EtOAc, organic layers were combined and dried with MgSO4 (anh), filtered off and concentrated. Crude was purified using silica gel cartridge with linear gradient 0-85% DCM/MeOH to yield the title compound (114 mg, 0.808 mmol, 50.1% yield) as yellow syrup. 1H NMR (300 MHz, DMSO-d6) δ ppm: 6.50-6.85 (m, 3H), 4.95-5.08 (m, 3H), 4.44 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524750B2
Source datasetuspto-grants-2013_09
ORD IDord-970e1aba485d4c99b3702526307d880f
Source noteuspto-grants-2013_09