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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226213Generated: October 25, 2026

3-Methoxybenzylamine → HCID 57754052, compound

https://huagongshe.com/reaction/226213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzylamineHCID 21156—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrifluoromethanesulfonic acid, lithium saltHCID 3664839—
Reactant(1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl esterHCID 86616462—
SolventAcetonitrileHCID 6342—
ProductHCID 57754052HCID 57754052—

Reaction Steps

A solution of (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester (0.03 g, 0.1 mmol) in acetonitrile (1 mL) was treated with lithium triflate (0.032 g, 0.2 mmol) and stirred at ambient temperature for 20 minutes. Then 3-methoxybenzylamine (0.016 mL, 0.12 mmol) was added to the reaction neat in one portion. The reaction was stirred at ambient temperature for 14 hours. The reaction was poured into saturated ammonium chloride solution (5 mL), extracted with ethyl acetate, the organic phase separated, dried (MgSO4) and the solvent removed at reduced pressure. The product was obtained as an oil and used without further purification (0.041 g, 94%). MS: 437 (M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557137B2
Source datasetuspto-grants-2009_07
ORD IDord-102b0fd138274c048ebe5de232edecef
Source noteuspto-grants-2009_07