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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885159Generated: October 25, 2026

Ammonium Chloride → (2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(4,4,4-trifluoro-3-phenyl-butyl)-2,5-dihydro-pyrazine

https://huagongshe.com/reaction/885159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 736066—
Reactant(3-Iodo-1-trifluoromethylpropyl)-benzeneHCID 67178112—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(4,4,4-trifluoro-3-phenyl-butyl)-2,5-dihydro-pyrazineHCID 67177689—

Reaction Steps

A solution of (R)-(−)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (1.1 g) in tetrahydrofuran (25 ml) was cooled to −70° C., then tert.butyllithium (1.7 M in pentane, 3.88 ml) was added and the mixture was stirred for 1 hour. A solution of (3-iodo-1-trifluoromethyl-propyl)-benzene (1.98 g) in tetrahydrofuran (7 ml) was added slowly and the mixture was stirred overnight at −70° C. At room temperature saturated ammonium chloride solution was added and the mixture was extracted three times with ether. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (SiO2, heptane/EtOAc=9:1 to yield a yellow liquid, (1.86 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242153B2
Source datasetuspto-grants-2012_08
ORD IDord-8b979149bfaf420d84f4f17b56e20eb0
Source noteuspto-grants-2012_08