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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165276Generated: November 1, 2026

Dibenzylamine → alpha-[[Bis(phenylmethyl)amino]methyl]-3-(methoxymethyl)-4-(phenylmethoxy)benzenemethanol

https://huagongshe.com/reaction/1165276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzylamineHCID 7656—
Reactant2-Bromo-1-[3-(methoxymethyl)-4-(phenylmethoxy)phenyl]ethanoneHCID 12498966—
SolventTetrahydrofuranHCID 8028—
Productalpha-[[Bis(phenylmethyl)amino]methyl]-3-(methoxymethyl)-4-(phenylmethoxy)benzenemethanolHCID 1986271785.9%

Reaction Steps

A solution of 2-bromo-1-[3-(methoxymethyl)-4-(phenylmethoxy)phenyl]ethanone (2.0 g), dibenzylamine (1.2 g) and DEA (0.8 g) in THF (30 ml) was allowed to stand at room temperature for 18 h, filtered and evaporated. The residual oil was dissolved in ethanol (20 ml) and treated portionwise with sodium borohydride (0.23 g), under nitrogen. The mixture was stirred at room temperature for 1 h, treated with methanol (20 ml), and evaporated. The residue was purified by FCC eluting with CX-ER (3:1) to give the title compound as an off-white solid (2.3 g), m.p. 52°-57°, t.l.c. (CX-ER 1:1) Rf 0.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908386
Source datasetuspto-grants-1990_03
ORD IDord-d6936fe54de6497bac92ee75bf19e192
Source noteuspto-grants-1990_03