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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497722Generated: October 30, 2026

4-Methoxybenzylamine → HCID 117600113, compound

https://huagongshe.com/reaction/1497722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant5-Bromo-2-hydroxybenzophenoneHCID 229009—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 136930497HCID 136930497—
SolventDichloromethaneHCID 6344—
ProductHCID 117600113HCID 117600113—

Reaction Steps

(5-Bromo-2-hydroxy-phenyl)-phenyl-methanone (5.0 g, 17.68 mmol) is dissolved in dichloromethane (20 mL). 4-Methoxybenzylamine (3.00 mL, 22.02 mmol) is added and the mixture stirred at room temperature for 2 hours. 4-Bromo-2-[(4-methoxy-benzylimino)-phenyl-methyl]-phenol (700 mg, 1.766 mmol) is dissolved in dichloromethane (6 mL) and treated with sodium triacetoxyborohydride (2.0 g, 8.96 mmol). The mixture is stirred at room temperature over the weekend. The mixture is poured into saturated aqueous sodium bicarbonate solution. The aqueous phase is exhaustively extracted with dichloromethane. The combined organic phases are dried over magnesium sulfate, the drying agent is filtered off. The filtrate is concentrated to dryness in vacuo. The residue is purified by column chromatography on silica gel using dichloromethane as an eluant. The product fractions are evaporated to dryness in vacuo. This affordes the desired compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199988B2
Source datasetuspto-grants-2015_12
ORD IDord-402beafc869547df9e3745f83b4f7e86
Source noteuspto-grants-2015_12