HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoquinoline-4-carbaldehyde → (Isoquinolin-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoquinoline-4-carbaldehyde | HCID 10868870 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Isoquinolin-4-yl)methanol | HCID 12746377 | — |
Reaction Steps
4-Isoquinolinecarboxaldehyde (1 mmole) (prepared by the method of: J. B. Wommack, T. G. Barbee, Jr., D. J. Thoennes, M. A. McDonald and D. E. Pearson, J. Heterocyclic Chem., 1969, 6, 243-245.) is dissolved in anhydrous THF (50 mL) and treated with borane-methyl sulfide (0.3 mmoles) (as described in: E. Mincione, J. Org. Chem., 1978, 43, 1829-1830) at 0° C. for 0.5-1 h and worked up in the usual way to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362188B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-577be0b0b84a42acb9d78e31bd6f4cc8 |
| Source note | uspto-grants-2002_03 |