HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epibromohydrin → 7-Phenylheptyloxymethyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzeneheptanol | HCID 154271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Phenylheptyloxymethyloxirane | HCID 21474764 | — |
Reaction Steps
A procedure similar to that described in Preparation 46 was repeated, except that 2 g of 7-phenylheptyl alcohol, 1.7 ml of epibromohydrin, 0.44 g of sodium hydride (as a 55% by weight dispersion in mineral oil) and 50 ml of anhydrous dimethylformamide were used, to give 1.15 g of the title compound having an Rf value of 0.49 (on silica gel thin layer chromatography, using a 1:6 by volume mixture of ethyl acetate and hexane as the developing solvent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688823 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-50711051149043619a8df4a049e26e6d |
| Source note | uspto-grants-1997_11 |