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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594799Generated: October 26, 2026

N-Methylaniline → 2-{3-[Methyl(phenyl)amino]phenyl}ethan-1-ol

https://huagongshe.com/reaction/594799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylanilineHCID 7515—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant(3-Bromophenethoxy)(tert-butyl)dimethylsilaneHCID 11515183—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-{3-[Methyl(phenyl)amino]phenyl}ethan-1-olHCID 1131071572%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-Bromo-3-[2-(tert-butyldimethylsilyloxy)ethyl]benzene (2.5 g, 7.96 mmol), N-methylaniline (1.02 g, 9.55 mmol), Pd2dba3 (364 mg, 0.4 mmol), Xantphos (691 mg, 1.19 mmol) and NaOtBu (727 mg, 9.55 mmol) were combined in toluene (12 mL), and the reaction was heated at 100° C. in the microwave for 90 min. The reaction was diluted with EtOAc, washed with brine, dried (MgSO4), and concentrated. The residue was stirred in 70% TFA/DCM (10 mL) for 2 h. The solution was concentrated and purified by silica gel chromatography (30% to 100% EtOAc/hexanes) to give 1.3 g (72%) of the title compound as a clear oil. 1H NMR (400 MHz, CDCl3): δ 1.53 (1H, br s), 2.81 (2H, t, J=6.5 Hz), 3.31 (3H, s), 3.83 (2H, t, J=6.5 Hz), 6.81 (1H, d, J=7.4 Hz), 6.86-6.89 (2H, m), 6.97 (1H, t, J=7.3 Hz), 7.04 (d, 2H, J=7.8 Hz), 7.18-7.29 (3H, m). [M+H] Calc'd for C15H17NO, 228. Found, 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242968B2
Source datasetuspto-grants-2016_01
ORD IDord-a58384bd48784cacac5f89cc5e34ae02
Source noteuspto-grants-2016_01