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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559284Generated: October 30, 2026

Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine → 1-[(3RS,4SR)-1-Benzyl-4-(2,4-difluoro-phenyl)-pyrrolidin-3-yl]-ethanone

https://huagongshe.com/reaction/559284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
Reactant(E)-4-(2,4-difluorophenyl)but-3-en-2-oneHCID 58310994—
CatalystTrifluoroacetic acidHCID 6422—
SolventDichloromethaneHCID 6344—
Product1-[(3RS,4SR)-1-Benzyl-4-(2,4-difluoro-phenyl)-pyrrolidin-3-yl]-ethanoneHCID 6699923989.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of N-(methoxymethyl)-N-(phenylmethyl)-N-(trimethylsilyl)methylamine (7.82 g, 32.9 mmol) in CH2Cl2 (40 mL) was added dropwise, over a 30 minutes period, to a stirred solution of (E)-4-(2,4-difluoro-phenyl)-but-3-en-2-one (4.0 g, 21.9 mmol) and trifluoroacetic acid (0.17 mL, 0.21 mmol) in CH2Cl2 (10 mL) at 0° C. The ice bath was removed, and the solution was stirred at 25° C. for an additional 48 h. It was then concentrated and purification by flash chromatography (SiO2, CH2Cl2/MeOH 98:2) afforded 6.2 g (89%) of the title compound as a yellow oil. ES-MS m/e: 316.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063075B2
Source datasetuspto-grants-2011_11
ORD IDord-e46eea457e0e496eade5ae5c0a9c283f
Source noteuspto-grants-2011_11