HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofurfuryl alcohol → [1,4]Benzodioxino[2,3-c]pyridazin-3-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl[1,4]benzodioxino[2,3-c]pyridazine-3-carboxylate | HCID 117695404 | — |
| Solvent | Water | HCID 962 | — |
| Product | [1,4]Benzodioxino[2,3-c]pyridazin-3-ylmethanol | HCID 117691161 | 66.6% |
Reaction Steps
To methyl[1,4]benzodioxino[2,3-c]pyridazine-3-carboxylate (950 mg) was added a mixed solvent of tetrahydrofuran-methanol (1:1) (20 ml), and the mixture was stirred under ice-cooling. To the mixture was added sodium borohydride (450 mg), and the mixture was stirred at 0° C. for 2 hr. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was washed with water to give [1,4]benzodioxino[2,3-c]pyridazin-3-ylmethanol (560 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212147B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-e2de03019b254c189317c4774b40a54c |
| Source note | uspto-grants-2015_12 |