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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640514Generated: November 2, 2026

Sodium borohydride → HCID 66736400, compound

https://huagongshe.com/reaction/1640514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Methoxyquinoxaline-5-carbaldehydeHCID 71607438—
SolventEthanolHCID 702—
ProductHCID 66736400HCID 6673640071.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of 3-methoxy-quinoxaline-5-carbaldehyde (4.05 g, 21.5 mmol; see WO 2006/032466) in EtOH (150 mL) cooled at 0° C., NaBH4 (814 mg, 21.5 mmol) was added in one portion. The reaction mixture was warmed to rt and stirred for 1 h. The mixture was quenched at 0° C. by addition of 1M HCl until H2 evolvement ceased, then concentrated under reduced pressure. The phases were separated between EA and sat. aq. NaHCO3, the org. layer was dried over MgSO4 and concentrated under reduced pressure. The residue was chromatographed on SiO2 (DCM-MeOH—NH4OH: 1000:50:4) to afford the title alcohol as a dark yellow solid (2.92 g, 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114867B2
Source datasetuspto-grants-2012_02
ORD IDord-ba87d30395664a4fb2055250c5ce0936
Source noteuspto-grants-2012_02