HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4,8-Dimethyl-1-(2-phenyl-1, 3-dioxolan-2-yl)-7-nonen-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Bromo-2-methyl-2-pentene | HCID 137521 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 5-(2-Phenyl-1,3-dioxolan-2-yl)-2-pentanone | HCID 22320897 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diethylether heptane | HCID 21897273 | — |
| Product | 4,8-Dimethyl-1-(2-phenyl-1, 3-dioxolan-2-yl)-7-nonen-4-ol | HCID 22320908 | 38% |
Reaction Steps
A Grignard reagent of 3.50 g (0.021 mol) of 5-bromo-2-methyl-2-pentene in 13 ml of ether and 0.62 g (0.026 mol) of magnesium turnings in 14 ml of ether was added slowly at −25° under N2 to a stirred solution of 5.54 g (0.024 mol) of 5-(2-phenyl-1,3-dioxolan-2-yl)-2-pentanone obtained under b) in 20 ml of ether. During the introduction, the temperature was left rising up to −5° C. and the reaction mixture left stirring for 45 min. Then a saturated solution of NH4Cl was added and the formation of a white precipitate was observed. Extraction with ether (2×), washing with water (3×), drying (Na2SO4) and concentrating gave 6.24 g of the crude product. Column chromatography (SiO2, heptane/ether 7:3) gave 2.53 g (38%) of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06949680B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-2a3227adadbc4419bb359f57eaef038b |
| Source note | uspto-grants-2005_09 |