HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-[1-(1-Imidazolyl)-butyl]-benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[1-(1-Imidazolyl)-butyl]-benzoic acid methyl ester | HCID 14514374 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[1-(1-Imidazolyl)-butyl]-benzyl alcohol | HCID 14514376 | 67.3% |
Reaction Steps
1.0 g of benzoic acid methyl ester of example 1 is dissolved in 15 ml of tetrahydrofuran and mixed with 0.15 g (3.9 mmol) of lithium aluminum hydride and left at room temperature for 1 hour. The reaction solution is mixed with 50% sodium hydroxide solution and the organic phase is decanted. The organic phase is concentrated by evaporation in a vacuum and distilled on a bulb tube, boiling point 200° C./0.03 mbar. 0.6 g of 4-[1-(1-imidazolyl)-butyl]-benzyl alcohol is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05045558 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-eeb44f335fc64700b49c974612552767 |
| Source note | uspto-grants-1991_09 |