HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 71093329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86676901 | HCID 86676901 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 71093329 | HCID 71093329 | 95% |
Reaction Steps
To an ice-cooled solution of 3-(3-(1,3-dioxolan-2-yl)propoxy)benzaldehyde (prepared as in Example 10; Step 1) (3.08 g, 13.1 mmol) in ethanol (66 mL), was added sodium borohydride (1.98 g, 52.4 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred at ambient temperature for 16 hours. The reaction mixture was carefully quenched with saturated aqueous ammonium chloride and extracted twice with DCM. The combined organic phases were poured through a hydrophobic column, and the solvent was evaporated at reduced pressure to afford the title compound as a colourless oil (2.96 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877774B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-4542960545264245a2d2563c0e8056c6 |
| Source note | uspto-grants-2014_11 |