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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356990Generated: November 2, 2026

Diethyl Ether → HCID 12074084, compound

https://huagongshe.com/reaction/1356990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 12074083HCID 12074083—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 178455855HCID 178455855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12074084HCID 1207408484%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Part A: 8-(2,4-dichlorophenyl)-2-ethyl-3-(1-hydroxybutyl)imidazo[1,2-a]pyrazine: The aldehyde (1.6 g, 5.0 mmol, Part D of Example 1) was dissolved in anhydrous THF (25.0 mL) and cooled to −78° C. under nitrogen. To this mixture was added dropwise 2.0 M n-PrMgCl in diethyl ether (6.7 mL, 14.4 mmol) and stirred at −78° C. for 4 h. TLC (1:10 MeOH/CH2Cl2) revealed absence of starting material spot (Rf=0.88) and showed a new spot at Rf=0.05. The reaction mixture was quenched with saturated NH4Cl (30.0 mL), stirred the mixture for 10 min., extracted with EtOAc (3×100 mL), dried (MgSO4) and concentrated in vacuum to afford yellow oil. The residue was purified by flash column chromatography on a silica gel using 2.5% MeOH/CH2Cl2 to afford 1.63 g (84%, mp 159-160° C.) of desired product as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589952B2
Source datasetuspto-grants-2003_07
ORD IDord-7acf3808dbd441c1884d99834af85f59
Source noteuspto-grants-2003_07