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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497520Generated: October 30, 2026

Methanol → HCID 90281909, compound

https://huagongshe.com/reaction/1497520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 90281957HCID 90281957—
CatalystCobalt(II) chlorideHCID 24288—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90281909HCID 9028190947.8%

Reaction Steps

To a mixed solution of tert-butyl 3-cyano-5-fluorobenzoate (3.00 g) in tetrahydrofuran (60.0 mL)-methanol (30.0 mL) was added a mixture of cobalt (II) chloride (4.40 g) and water (60.0 mL) under ice-cooling, and then sodium borohydride (1.54 g) was added under an argon flow, followed by stirring at room temperature for 30 minutes. The insoluble material was filtered through Celite and then washed with a mixed solvent of tetrahydrofuran-methanol-water (2:1:2, and then the filtrate was concentrated under reduced pressure. To the residue was added a saturated aqueous sodium chloride solution, followed by extraction with chloroform. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (chloroform-methanol) to obtain tert-butyl 3-(aminomethyl)-5-fluorobenzoate (1.46 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199927B2
Source datasetuspto-grants-2015_12
ORD IDord-803e3454c74c4a19b019e1b7626324b6
Source noteuspto-grants-2015_12