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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395758Generated: October 25, 2026

Sodium borohydride → 3-Benzyloxy-4-methyl-phenylamine

https://huagongshe.com/reaction/395758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Benzyloxy-1-methyl-4-nitro-benzeneHCID 18174502—
CatalystNickel acetate tetrahydrateHCID 62601—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyloxy-4-methyl-phenylamineHCID 279462597%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-benzyloxy-4-methylnitrobenzene (1.1 g, 4.4 mmol) in tetrahydrofuran (25 mL) and methanol (50 mL) was added nickel acetate tetrahydrate (2.2 g, 8.7 mmol). The solution was cooled to 0° C. and sodium borohydride (0.66 g, 17.4 mmol) was added in small portions. After gas evolution had ceased, the solvents were removed in vacuo and the residue was partitioned between ethyl acetate and concentrated ammonium hydroxide. The layers were separated and the organic phase was washed with ammonium hydroxide followed by saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated In vacuo to give 0.9 g (97%) of the title product as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605626B2
Source datasetuspto-grants-2003_08
ORD IDord-45acb0023692450f80e5692efd70658b
Source noteuspto-grants-2003_08