HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanol → 2-Bromobenzyl cyclohexyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromobenzyl cyclohexyl ether | HCID 11173233 | 99% |
Reaction Steps
1.2 g of sodium hydride at 50% in suspension in oil are added at 5° C., in portions, to 5 g of cyclohexanol in solution in 150 ml of dimethylformamide. The mixture is stirred for 1 hour at room temperature and 12.5 g of 2-bromobenzyl bromide in solution in 15 ml of dimethylformamide are introduced at 5° C. After 2 hours at room temperature, the reaction medium is poured over ice-cold water and extracted with ethyl acetate. The organic phase is dried over anhydrous sodium sulfate and evaporated to give 13.3 g of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07288659B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-6b03538b6dbd41919e931e1004f5a61e |
| Source note | uspto-grants-2007_10 |