HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1,3-Dichloro-3-fluoro-7-oxabicyclo[4.1.0]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2,6-Trichloro-6-fluorocyclohexanol | HCID 18970960 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dichloro-3-fluoro-7-oxabicyclo[4.1.0]heptane | HCID 18970966 | — |
Reaction Steps
0.85 g (21.3 mmol) of sodium hydroxide pellets were added in three portions to 1.6 g (7.22 mmol) of pure alcohol 1f in suspension in 22 cm3 of distilled water at 15°-20° C. The reaction mixture was kept at room temperature for 1 h 15 min, 10 cm3 of ether were then added, stirring was continued for 5 min and then the aqueous phase was separated off and extracted with ether (5×25 cm3). The ether phases were combined, dried over magnesium sulfate and filtered, and the solvent was evaporated off. 1.28 g of a liquid, the epoxide 2e, were obtained; the crude yield was 96% (macrobore GC purity>98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424460 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-5012092a33f94258a496fa5a096d1aad |
| Source note | uspto-grants-1995_06 |