HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 5-(1-Cyclopentenyl)pentan-2-one | HCID 13528009 | — |
| Product | 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol | HCID 18433873 | 11% |
Reaction Steps
5-(Cyclopent-1-enyl)-2-pentanone (5.95 g; 39 mmol) in ethyl ether (6 ml) was added dropwise to a 3M solution of methylnagnesium bromide in the same solvent (17 ml; 51 mmol) during 15 minutes. After 2 hours at reflux, the mixture was cooled down to room temperature, poured into ice (20 g), acidified with 5N HCl (20 ml) and extracted with MTBE (60 ml). The aqueous phase was separated and extracted again with MTBE (2×100 ml). The combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml), dried over MgSO4 and concentrated in vacuo. Bulb-to-bulb distillation (80° C./0.06 torr) yielded quantitatively 5.84 g of 5-(cyclopent-1-enyl)-2-methylpentan-2-ol containing 11% of 5-cyclopentylidene-2-methylpentan-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410000B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-13540fe1e8c841bc8238ffba1ff52f14 |
| Source note | uspto-grants-2002_06 |