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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520778Generated: October 29, 2026

2-Propylquinoxaline → HCID 73507581, compound

https://huagongshe.com/reaction/520778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropylquinoxalineHCID 13283007—
SolventTolueneHCID 1140—
ProductHCID 73507581HCID 7350758196.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

To an argon-purged pressure-resistant glass vessel (100 mL) equipped with a magnetic stir bar, RuCl[(R)-daipena][(R)-dm-segphos] (1.6 mg, 1.4 μmol) and KO(t-Bu) (8.0 mg, 0.071 mmol) were added, and the vessel was purged with argon again. To this vessel, a toluene (1.4 mL) solution containing 2-(1-propyl)quinoxaline (238.5 mg, 1.38 mmol) and being degassed by the freeze-pump-thaw technique in advance was added by pressure transfer using a cannula. An operation in which hydrogen was introduced into the pressure-resistant vessel up to 0.8 MPa and then released was repeated 10 times to completely substitute the inside with hydrogen. Then, hydrogen was introduced up to 2.0 MPa, and the vessel was stirred in a water bath at 40° C. for 28 hours. After hydrogen was released, the solution was concentrated under reduced pressure, and the residue was purified through a silica gel short path column (ethyl acetate) to obtain (S)-1,2,3,4-tetrahydro-2-(1-propyl)quinoxaline (235.4 mg, 96%). A result of an analysis conducted by high performance liquid chromatography (column: CHIRALCEL OD-H, mobile phase: hexane:IPA=80:20, 1 mL/min) showed that the optical purity of this product was 99% ee or higher.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328079B2
Source datasetuspto-grants-2016_05
ORD IDord-385de7e3783c4cbf9470e65ce61a5c2b
Source noteuspto-grants-2016_05