HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Acetate hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium 2-methylbutan-2-olate | HCID 2733478 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetate hexane | HCID 22139250 | 95% |
Reaction Steps
0.38 ml of a 1.5M solution of sodium tert-amylate in benzene is added to 126 mg of the mesylate lactone obtained at stage A in 2 ml of anhydrous tetrahydrofuran, at 0° c. The temperature is allowed to rise to 20° C. over 15 minutes. After hydrolysis, extraction is done with ether, then the organic phase is washed with salt water. After chromatographing on a silica column (eluent acetate-hexane 40/60), 73 mg of the cis-cyclopropane lactone expected is obtained. (Yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04610826 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-484cd442d8b3498689e72dba8be8b6cf |
| Source note | uspto-grants-1986_09 |