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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid ethyl ester | HCID 67177112 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid methoxy-methyl-amide | HCID 86638533 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242153B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-c331964ce7a8470ab864976039665d16 |
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| Source note | uspto-grants-2012_08 |
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