HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (1r)-2-Imidazolyl-1-phenylethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | (+)-Styrene oxide | HCID 114705 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1r)-2-Imidazolyl-1-phenylethan-1-ol | HCID 69735309 | 32% |
Reaction Steps
In a manner similar to that of Example 49, step 1, imidazole (2.83 g, 41.6 mmol) is dissolved in absolute ethanol (45 mL). Pyridine (0.11 mL) is added followed by addition of (R)-(+) styrene oxide (5.0 g, 41.6 mol, Aldrich Chemical Co.), followed by heating at reflux for 18 hours. The mixture is evaporated in vacuo to a syrup and suspended between ethyl ether (250 mL) and water (100 mL) to give a solid precipitate. The suspension is filtered and washed with ethyl ether. The solid is recrystallized from hot ethyl acetate and dried in vacuo (2.52 g, 32% yield). MS: APCI: M+1, 189.1 (M: 188.2). NMR spectrum is consistent with structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943183B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-150e80cf7b2f4adaa9053a82b1eba305 |
| Source note | uspto-grants-2005_09 |