HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Product | 1-Phenylethanol | HCID 7409 | 163.8% |
Reaction Steps
2-Propanol (1.53 ml, 20 mmol) was added to 9.9 ml (10 mmol) of a toluene solution of DIBAH (1.02 M) at room temperature and the mixture was stirred at room temperature for 1 hour. Thereto was added 0.601 g of acetophenone, and the resultant mixture was stirred at room temperature for 6 hours, followed by hydrolysis with 1 N hydrochloric acid with ice cooling. Extraction with ethyl acetate and concentration gave 1.001 g of α-phenethyl alcohol as an oil. Conversion 55%, yield 47.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150567 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-de774cd4c4ce4789959980b7f1c5dddf |
| Source note | uspto-grants-2000_11 |