HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-isoquinolinecarboxylate → Isoquinoline-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-isoquinolinecarboxylate | HCID 725374 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Isoquinoline-3-carboxaldehyde | HCID 231555 | 85.7% |
Reaction Steps
3-Isoquinolinecarboxaldehyde (7 g, 84%) was prepared by reduction of 3-isoquinolinecarboxylic acid methyl ester (10 g, 52 mmol) with 1M LAH (27 ml in THF, 27 mmol) in 300 ml of dry THF at -78° C. for 30 minutes. The mixture was quenched with 7 ml of acetic acid, concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate, 2:1) to afford 7 g (84%) of 3-iso-quinolinecarboxaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554620 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-5523d22bbb1c43b4bc07ab65d3251fe7 |
| Source note | uspto-grants-1996_09 |