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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888950Generated: October 29, 2026

Sodium borohydride → N-(5-methyl-2-(3,4,5-trimethoxybenzylamino)phenyl)benzamide

https://huagongshe.com/reaction/1888950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178492111HCID 178492111—
SolventMethanolHCID 887—
ProductN-(5-methyl-2-(3,4,5-trimethoxybenzylamino)phenyl)benzamideHCID 68517409—

Reaction Steps

A suspension of compound (E)-N-(5-methyl-2-(3,4,5-trimethoxybenzylideneamino)phenyl)benzamide (3 mmol) in methanol was cooled with an ice bath. Sodium borohydride was added until the color turned white. Excess sodium borohydride was quenched by the addition of distilled water. The resulting mixture was extracted with ethyl acetate (50 mL×3). The combined organics were washed with brine, dried over anhydrous MgSO4, and concentrated in vacuum to obtain N-(5-methyl-2-(3,4,5-trimethoxybenzylamino)phenyl)benzamide as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501957B2
Source datasetuspto-grants-2013_08
ORD IDord-651f6ba5cbf34505aef966ad6a8c237b
Source noteuspto-grants-2013_08