HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epibromohydrin → 2-{2-[4-(2-Chlorophenyl)butyl]phenoxymethyl}oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | 2-[4-(2-Chlorophenyl)butyl]phenol | HCID 19423957 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-{2-[4-(2-Chlorophenyl)butyl]phenoxymethyl}oxirane | HCID 19423926 | 88.5% |
Reaction Steps
Following a procedure similar to that described in Example 1(a), 800 mg of 2-[4-(2-chlorophenyl)butyl]phenol (prepared as described in Preparation 18), 344 mg of potassium t-butoxide and 835 mg of epibromohydrin were reacted in 20 ml of dimethylacetamide. The crude product, extracted as described in Example 1(a), was purified as described in Example 1(a), to give 860 mg (yield 88%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556864 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-3fc4a683d5784079aacd923c9d62ffc6 |
| Source note | uspto-grants-1996_09 |