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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983227Generated: October 30, 2026

Lithium → N-methyl-2-phenoxyaniline

https://huagongshe.com/reaction/1983227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithiumHCID 3028194—
ReactantHCID 65142714HCID 65142714—
SolventTetrahydrofuranHCID 8028—
ProductN-methyl-2-phenoxyanilineHCID 2296195594.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 2-phenoxy-N-(t-butoxycarbonyl)aniline (1.43 g, 5.0 mmol) in anhydrous tetrahydrofuran (50 ml) was added lithium aluminumhydride (10 ml, 10.0 mmol, 1.0 M solution in tetrahydrofuran) at −10° C. The mixture was then refluxed at 65° C. overnight. The reaction mixture was quenched with slow addition of MeOH (10 ml) and concentrated under reduced pressure. The reaction mixture was then poured into water (50 ml) and extracted with ethyl acetate (3×100 ml). Organic extracts were combined and washed with brine (2×100 ml) and dried over (Na2SO4), concentrated under reduced pressure to give N-methyl-2-phenoxyaniline (0.94 g, 94.0%) as a pale yellow oil. The product was confirmed by LC-MS and subjected to next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541373B2
Source datasetuspto-grants-2009_06
ORD IDord-89cc1c884c8744dfa0cb31b4ec121668
Source noteuspto-grants-2009_06