Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 13479951 | HCID 13479951 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19005530 | HCID 19005530 | — |
Reaction Steps
A solution of 8.5 g of p-dibromobenzene in 35 ml of anhydrous diethyl ether was added dropwise under stirring at 15°-20° C. to 1 g of magnesium metal powder, followed by reaction at room temperature for 1 hour so that a Grignard reagent was formed. After 5 g of 4-pentylcyclohexenone were added under stirring at -10° to 0° C. to the thus-formed Grignard reagent, they were reacted at room temperature for additional 1 hour. After the completion of the reaction, diluted hydrochloric acid was added dropwise to the reaction mixture, followed by the extraction of the reaction mixture with diethyl ether. After the extract was washed with saturated NaCl, anhydrous sodium sulfate was added to dry the extract. The diethyl ether was distilled off under reduced pressure, whereby 4-(4-bromophenyl)-4-hydroxy-1-pentylcyclohexene was obtained as a crude reaction product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05342546 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-120902810b9a484f915edad38de65088 |
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| Source note | uspto-grants-1994_08 |
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