HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-methyl-2-pentene → 3-(4-Methylpent-3-en-1-yl)cyclopent-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-methyl-2-pentene | HCID 137521 | — |
| Reactant | 3-Methoxycyclopent-2-en-1-one | HCID 643476 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(4-Methylpent-3-en-1-yl)cyclopent-2-en-1-one | HCID 21881144 | 65% |
Reaction Steps
Magnesium turnings 2.1 g (0.086 mole) were added to 50 ml diethyl ether with stirring. 1-Bromo-4-methyl-3-pentene 10 g (0.061 mole) was added dropwise over 30 minutes. The reaction was allowed to warm from 25° C. to 40° C. during the addition and aged for 30 minutes. A solution of 3-Methoxy-2-cyclopenten-1-one, 10 g (0.089 mole) in diethyl ether was added at 25° C. The resulting mixture was aged 30 minutes then quenched with 20% aqueous acetic acid (50 ml). The organic layer was dried over sodium sulfate, filtered and distilled to give 6.6 g (65% yield) of 3-(4-methyl-3-pentenyl)-2-cyclopenten-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531696B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-47c9d1c71f54417888aa6426d0af99be |
| Source note | uspto-grants-2009_05 |