HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-[4-Hydroxy-4-(4-t-butylphenyl)butyl]imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole | HCID 20282496 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[4-Hydroxy-4-(4-t-butylphenyl)butyl]imidazole | HCID 13457363 | — |
Reaction Steps
To a 0° C. solution of 5.0 g of the above ketone in 150 ml. of anhydrous methanol was added excess sodium borohydride and the mixture stirred for one hour. After removal of the solvent, a small quantity of water was added and the mixture was extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and evaporated to afford 1-[4-hydroxy-4-(4-t-butylphenyl)butyl]imidazole, which was converted to the oxalate salt and recrystallized from ethyl acetate/ethanol, m.p. 205°-207° C.(foaming).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518607 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-ac368a735b4f46a5a7d9f55a361b33df |
| Source note | uspto-grants-1985_05 |