Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741570Generated: October 31, 2026

Ethylene Oxide → HCID 19426627, compound

https://huagongshe.com/reaction/741570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
ReactantPotassium CarbonateHCID 11430—
Reactant491-40-7HCID 244861—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19426627HCID 1942662755%

Reaction Conditions

Temperature-65 °C

Reaction Steps

A stirred solution of diisopropylamine (2.25 ml, 0.016 mole) in dry THF (20 ml) at -50° C. under nitrogen was treated with 1.6M n-butyllithium in hexane (9.4 ml, 0.015 mole). After 10 minutes the solution was cooled to -65° C. and treated with a solution of quinolizidin-4-one (I. Murakoshi, Yakugaku Zasshi, 1958, 78, 594) (2.0 g, 0.013 mole) in ether (20 ml), stirred for a further 10 minutes and then ethylene oxide (1.23 g, 0.028 mole) bubbled into the solution, which was allowed to warm to room temperature over 1 hour and then heated under reflux for 1.5 hours. The reaction mixture was treated with concentrated potassium carbonate solution (30 ml) and extracted with ethyl acetate (2×60 ml). The combined extracts were dried (Na2SO4), concentrated in vacuo and the residue chromatographed on silica gel eluting with chloroform/methanol (98:2) to afford 3-(2-hydroxyethyl)quinolizidin-4-one as a pale yellow oil (1.4 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552398
Source datasetuspto-grants-1996_09
ORD IDord-39e5c765a21f4424a1db13fea235112b
Source noteuspto-grants-1996_09