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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911565Generated: October 30, 2026

Trifluoroacetic acid → (2S,4S)-Methyl 2-amino-4-phenylhexanoate

https://huagongshe.com/reaction/1911565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
Reactant(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-((S)-2-phenyl-butyl)-2,5-dihydro-pyrazineHCID 66705866—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(2S,4S)-Methyl 2-amino-4-phenylhexanoateHCID 6670588885%

Reaction Steps

To a solution of trifluoroacetic acid (3.4 ml) in water (440 ml) was added dropwise over 15 min a solution of (2R,5S)-2-isopropyl-3,6-dimethoxy-5-((S)-2-phenyl-butyl)-2,5-dihydro-pyrazine (4.69 g, 14.8 mmol) in acetonitrile (75 ml). The mixture was stirred overnight at room temperature then made basic by addition of saturated aqueous sodium carbonate solution and the mixture was extracted with ethyl acetate. The phases were separated and the organic phase was washed sequentially with water and with saturated brine, then dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, EtOAc/heptane) to yield a yellow oil (2.78 g, 85%); MS (ISP): 222.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-7af8b51afbe44b5a8212f34f3f4933a6
Source noteuspto-grants-2013_12