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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172641Generated: October 31, 2026

Aluminium lithium hydride → (2,4-Difluoro-5-methylphenyl)methanol

https://huagongshe.com/reaction/2172641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 55264252HCID 55264252—
SolventTetrahydrofuranHCID 8028—
Product(2,4-Difluoro-5-methylphenyl)methanolHCID 45090665117.8%

Reaction Steps

To a solution of 2,4-difluoro-5-methyl-benzoic acid methyl ester from Step A (1.0 g, 5.37 mmol) in tetrahydrofuran (10 mL), cooled to −78° C. using a dry ice/acetone bath, was added lithium aluminum hydride, 1.0M in tetrahydrofuran (10 mL, 10 mmol), in a dropwise manner. The solution was stirred for two hours. The reaction was quenched by dropwise addition of ice-cold saturated sodium bicarbonate solution, allowed to warm to room temperature and was extracted with ethyl acetate. The organic layer was washed with water and brine and dried over magnesium sulfate. The slurry was filtered and concentrated to provide the alcohol as a colorless liquid (1.0 g, quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056110B2
Source datasetuspto-grants-2015_06
ORD IDord-c5f583ada7034ca280d25d90fcbbd195
Source noteuspto-grants-2015_06