HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 1-(1H-imidazol-1-yl)-3-methyl-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 1,2-Epoxy-3-methylbutane | HCID 102618 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(1H-imidazol-1-yl)-3-methyl-2-butanol | HCID 22324700 | 46% |
Reaction Steps
A solution of 2-isopropyloxirane (2.28 g, 26 mmol) and imidazole (1.80 g, 26 mmol) in acetonitrile (25 mL) was stirred at reflux for 16 h. The mixture was concentrated, and the residue was purified by flash column chromatography (SiO2, CH2Cl2-methanol-ammonium hydroxide 80:20:1) to give 1-(1H-imidazol-1-yl)-3-methyl-2-butanol as a yellow oil, 1.88 g, 46% yield. NMR spectrum was consistent with structure. MS EI: M+• 154.1103 (M+• −154.1106). 4. 6-hydroxy-5-[(phenylsulfonyl)methyl]-3,4-dihydro-1(2H)-naphthalenone
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943183B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-a76fd5db663444ac9ce001ed4653921c |
| Source note | uspto-grants-2005_09 |