HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (6-Chloropyridazin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Chloropyridazine-3-carbaldehyde | HCID 22336267 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (6-Chloropyridazin-3-yl)methanol | HCID 20557609 | — |
Reaction Steps
To a suspension of 6-chloropyridazine-3-carbaldehyde (2.50 g, 17.5 mmol) in 30 mL of methanol (30 mL) at 0° C. was added sodium borohydride (0.26 g, 7.02 mmol). The reaction mixture was warmed to room temperature. After 2 hours, the reaction mixture was concentrated in vacuo and triturated with 20% MeOH in dichloromethane to provide (6-chloropyridazin-3-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293914B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-d75aebc425c6462592b75a9d4a61eee8 |
| Source note | uspto-grants-2012_10 |