HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylacetic Acid → beta-Phenylphenethyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylacetic Acid | HCID 8333 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | beta-Phenylphenethyl alcohol | HCID 74662 | 90% |
Reaction Steps
To a rapidly stirring solution of 8.5 g (40 mmol) diphenyl acetic acid in 100 mL dry THF, at room temperature, was added 3.04 g (80 mmol) of LAH. The suspension was stirred at room temperature for 1 hour and then cooled to 0 degrees C. The excess LAH was decomposed by slow addition of 10% NaOH (200 mL aqueous solution). The product was extracted with AcOEt, dried over MgSO4 and concentrated under vacuum to yield 7.1 g (90%) of 2,2-diphenyl ethanol (12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04992421 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-07b91252976543058352788b7cc48a8c |
| Source note | uspto-grants-1991_02 |