HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-(2-Phenyl-chroman-6-yloxy)-1-propyl-cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(2-Phenyl-chroman-6-yloxy)-cyclohexanone | HCID 90390155 | — |
| Reactant | HCID 178455855 | HCID 178455855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Phenyl-chroman-6-yloxy)-1-propyl-cyclohexanol | HCID 90390004 | — |
Reaction Steps
100 mg of 4-(2-phenyl-chroman-6-yloxy)-cyclohexanone were dissolved at room temperature in 5 ml of tetrahydrofuran. A 2M solution of propylmagnesium chloride in diethyl ether (0.31 ml, 2 eq) was added, and stirring at room temperature was continued for 4 h. The reaction was stopped by careful addition of saturated aqueous ammonium chloride solution. The aqueous layer was extracted with methyl tert-butyl ether. The organic layer was dried over sodium sulfate and filtered, and the solvent removed by evaporation. The resulting oil was chromatographed over silica gel using heptane/ethyl acetate 20:1 as the eluent. 54 mg of the title compound were isolated as a pale yellow oil (48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440941B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-81069c4c704e42ddb46130f780f09869 |
| Source note | uspto-grants-2016_09 |