HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 4-chloro-2-ethyl-5-{[(phenylmethyl)oxy]methyl}-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-{1-cyano-2-[(phenylmethyl)oxy]ethyl}propanamide | HCID 59451375 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-chloro-2-ethyl-5-{[(phenylmethyl)oxy]methyl}-1H-imidazole | HCID 59451637 | 64.2% |
Reaction Steps
A solution of N-{1-cyano-2-[(phenylmethyl)oxy]ethyl}propanamide (3.62 g, 15.6 mmol), triphenylphosphine (10.2 g, 39.0 mmol), and carbon tetrachloride (3.8 mL, 39.0 mmol) in acetonitrile (150 mL) was heated at 45° C. for 4.5 h. The reaction was concentrated and the residue was stirred in CH2Cl2 (170 mL) and 0.5 N NaOH (150 mL) for 15 min. The organic layer was isolated, dried (Na2SO4), filtered, concentrated and the residue was purified by silica gel flash column chromatography (5-50% EtOAc:hexanes) to give the title compound (2.51 g, 64%) as a light yellow solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.29-7.38 (m, 5H), 4.52 (s, 2H), 4.50 (s, 2H), 2.65 (q, 2H), 1.26 (t, 3H). ES-LCMS: m/z 250.6, 252.9 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-12cf6e9dc7f347a6ba91c7196a7d8d8f |
| Source note | uspto-grants-2012_11 |