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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460161Generated: October 29, 2026

Diisobutylaluminum hydride → ((1r)-1-Phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amine

https://huagongshe.com/reaction/460161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactantn-((1r)-1-Phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamideHCID 20803221—
SolventTolueneHCID 1140—
Product((1r)-1-Phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amineHCID 60010447—
Product4-(5-{[((1r)-1-Phenylethyl)amino]methyl}-2-methylphenyl)phenolHCID 60010545—

Reaction Steps

To a solution of N-((1R)-1-phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamide (0.12 g, 0.34 mmol) in 10 mL of toluene was added DIBAL-H (1 mL, 1.5 mmol). The reaction was then heated to 100 C for 16 hours and cooled to RT. The reaction was quenched with 5 mL of 2N NaOH aq. soln. 100 mL of CH2Cl2 was used to extract the product. The organic phase was washed with 30 mL of brine, dried over Na2SO3 and concentrated in vacuo. The desired products were separated by silica gel column chromatography (30% to 60% EtOAc in hexane) provide ((1R)-1-phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amine and 4-(5-{[((1R)-1-phenylethyl)amino]methyl}-2-methylphenyl)phenol, which were treated with 1N HCl in Et2O separately to provide the HCl salts as white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196102B2
Source datasetuspto-grants-2007_03
ORD IDord-4f50dfc6c2ab4eca808610df41543d8e
Source noteuspto-grants-2007_03