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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885174Generated: October 29, 2026

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

https://huagongshe.com/reaction/885174

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 numberUS08242153B2
Source datasetuspto-grants-2012_08
ORD IDord-c331964ce7a8470ab864976039665d16
Source noteuspto-grants-2012_08