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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261093Generated: November 3, 2026

Quinoxaline-6-carbonyl chloride → Quinoxaline-6-carboxaldehyde

https://huagongshe.com/reaction/2261093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoxaline-6-carbonyl chlorideHCID 2776328—
ReactantLithium tritertbutoxyaluminohydrideHCID 16684435—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductQuinoxaline-6-carboxaldehydeHCID 76395873%

Reaction Steps

In a 1 l 3-neck flask under argon was placed Quinoxaline-6-carbonyl chloride in 600 ml of DME. To this solution was added lithium tri-tert-butoxyaluminohydride (1 eq.) at −78° C. over 1.5 h. The reaction was kept at that temperature for 5 h. Then ice was added, and the reaction was diluted with AcOEt and filtrated over celite. The two layers were separated and the organic phase was washed with NaHCO3 sat. Quinoxaline-6-carbaldehyde was obtained upon evaporating the solvent in 73% yield as yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846925B2
Source datasetuspto-grants-2010_12
ORD IDord-1d4c3883e1914f32958bfcf48f5aa66b
Source noteuspto-grants-2010_12