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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633935Generated: October 30, 2026

Aluminium lithium hydride → (5-Amino-2-trifluoromethoxy-phenyl)-methanol

https://huagongshe.com/reaction/1633935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 5-amino-2-(trifluoromethoxy)benzoateHCID 22061155—
SolventTetrahydrofuranHCID 8028—
Product(5-Amino-2-trifluoromethoxy-phenyl)-methanolHCID 2231114093.2%

Reaction Steps

5-Amino-2-trifluoromethoxybenzoic acid methyl ester (3.0 g, 12.8 mmol) was dissolved in THF (20 mL) in a three-necked flask equipped with a thermometer and an addition funnel under nitrogen. Under stirring and ice-cooling lithium aluminum hydride (1M in THF, 15 mL) was added dropwise within 10 minutes. Stirring was continued at room temperature for 1 hr, and the reaction was concentrated in vacuo. The residue was suspended in dichloromethane (150 mL) and water (50 mL), then filtered through celite, washed with dichloromethane and water. The filtrate was separated, and the water phase was extracted once more with dichloromethane (30 mL). The combined organic phases were washed with water (2×20 mL), dried (MgSO4) and concentrated in vacuo to give 2.47 g of (5-amino-2-trifluoromethoxyphenyl)methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-748f357d6c1347eabb418800da46ce49
Source noteuspto-grants-2003_01