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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178381Generated: October 29, 2026

Sodium borohydride → (4-(Cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamine

https://huagongshe.com/reaction/2178381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(Cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzonitrileHCID 118113961—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventEthanolHCID 702—
Product(4-(Cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamineHCID 11811399599%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred 0° C. solution of 4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzonitrile (2.50 g, 8.06 mmol) in ethanol (20 mL) was added cobalt(II) chloride hexahydrate (2.20 g, 9.25 mmol) in small portions. The resulting mixture was allowed to stir at 0° C. After 30 min, the mixture was treated with sodium borohydride (1.80 g, 47.58 mmol) added in small portions. The mixture was allowed to warm to room temperature. After 30 min, the mixture was filtered through Celite, and the filtercake was washed with ethanol (20 mL). The filtrate was concentrated to provide 2.50 g (99%) of (4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067914B1
Source datasetuspto-grants-2015_06
ORD IDord-19cbe9ef0e094d81ba3d4467ce637482
Source noteuspto-grants-2015_06