HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoxaline-6-carbonyl chloride → Quinoxaline-6-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoxaline-6-carbonyl chloride | HCID 2776328 | — |
| Reactant | Lithium tritertbutoxyaluminohydride | HCID 16684435 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Quinoxaline-6-carboxaldehyde | HCID 763958 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846925B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-1d4c3883e1914f32958bfcf48f5aa66b |
| Source note | uspto-grants-2010_12 |