HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-[1-hydroxy-2-(1-trityl-1H-imidazol-4-ylmethoxy)ethyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrile | HCID 66782326 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[1-hydroxy-2-(1-trityl-1H-imidazol-4-ylmethoxy)ethyl]benzonitrile | HCID 66782189 | — |
Reaction Steps
Sodium borohydride is added in portions to a solution of 1 mmol of 4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrile in 12 ml of ethanol at 0° C. The reaction solution is stirred at room temperature for 12 hours, then poured into ice-water and stirred for 15 minutes. The mixture is adjusted to pH 5 by adding glacial acetic acid and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried over sodium sulphate and evaporated. The title compound is identified from the residue on the basis of the Rf by flash chromatography (SiO2 60F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879847B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-be2ee89089ec47aaa9946c0d29187221 |
| Source note | uspto-grants-2011_02 |