HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21553303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(4-Acetylphenyl)furan-2-carbonitrile | HCID 21553321 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | HCID 21553303 | HCID 21553303 | 58% |
Reaction Steps
A solution of 46 g (0.22 mole) of 5-(4-acetylphenyl)-2-furonitrile in 800 ml of 95% dioxane/H2O was treated portionwise with 8.3 g (0.22 mole) of NaBH4 while keeping the temperature below 20° by means of an ice bath. The resulting solution was stirred at ambient temperature for 21/2 hours and then added to an ice/H2O mixture. After standing 48 hours, the reaction mixture was extracted with ether and the combined ethereal extracts dried over MgSO4. The ether was removed on the Calab evaporator yielding 27 g (58%) of product as a residual oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946049 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-1e4ddf3d09834c9ba1ffe986b44a8551 |
| Source note | uspto-grants-1976_03 |