HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 15524188, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 21253084 | HCID 21253084 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15524188 | HCID 15524188 | 62.2% |
Reaction Steps
A solution of the product from Example 5 (1 g, 3.24 mmol) and benzaldehyde (0.71 mL, 7 mmol) in 2:1 MeOH/H2O (50 mL) was treated with sodium cyanoborohydride (0.56 g, 9 mmol) portionwise under nitrogen and stirred for six hours. The reaction mixture was then added to dichloromethane (150 mL) and washed with saturated sodium bicarbonate. The organic layer was dried over magnesium sulfate and activated charcoal, filtered through a plug of silica gel and concentrated under vacuum to dryness. The solids were triturated in hexane, filtered, and oven dried to give the title compound (0.73 g, 62% yield) as an orange solid, mp=150-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057313 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-f93e578a7cf54e1da69895f8eaeda361 |
| Source note | uspto-grants-2000_05 |