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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026124Generated: October 31, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → 4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid methoxy-methyl-amide

https://huagongshe.com/reaction/1026124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid ethyl esterHCID 67177112—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid methoxy-methyl-amideHCID 86638533—

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a stirred solution of 4-(4-fluoro-phenyl)-4-methyl-pentanoic acid ethyl ester (3.97 g) and N,O-dimethylhydroxylamine hydrochloride (2.44 g) in tetrahydrofuran (40 ml) at −18° C. was added dropwise a solution of isopropylmagnesium chloride (25.0 ml, 2 M solution in THF). The mixture was stirred for 30 min at −15° C. and then quenched by addition of saturated ammonium chloride solution. The mixture was then acidified to pH 1 by addition of 1 M aq. hydrochloric acid and taken up in ethyl acetate. The mixture was washed sequentially with water and with saturated brine, then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (3.91 g, 93%); MS (ISP): 254.2 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729113B2
Source datasetuspto-grants-2014_05
ORD IDord-511d620eb24b4688878750b84d784df4
Source noteuspto-grants-2014_05