HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 5328503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Phenyl-1H-benzimidazol-5-ol | HCID 667662 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 5328503 | HCID 5328503 | — |
Reaction Steps
A solution of 5-hydroxy-1-phenylbenzimidazole (Example 14) (0.24 g, 1.14 mmol) 1:1 THF/DMF (5 mL) was added under nitrogen to a stirred suspension of sodium hydride (41 mg of a 60% dispersion in oil, 1.71 mmol). After 5 minutes, epichlorohydrin (98 μL, 1.26 mmol) was added, and the solution was refluxed for 4 hours. The cooled solution was partitioned between diethyl ether and water, and the extract was washed with 2N NaOH and worked up to give an oil which was chromatographed on silica gel. EtOAc/petroleum ether (1:1) eluted foreruns, while EtOAc eluted the epoxide Example 34 (0.14 g, 46%): mp (EtOAc/petroleum ether) 96-97.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990146 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-ce5c2d6bccd54421be09c139cfd79ee3 |
| Source note | uspto-grants-1999_11 |