HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992179Generated: October 26, 2026
2-Methoxy-6-(4-propylcyclohexenyl)naphthalene → HCID 178447821, compound
https://huagongshe.com/reaction/992179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxy-6-(4-propylcyclohexenyl)naphthalene | HCID 21869390 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178447821 | HCID 178447821 | 61.9% |
Reaction Steps
44.9 g of 2-methoxy-6-(4-propylcyclohexa-1-ene-1-yl)naphthalene was dissolved in 800 ml of ethyl acetate. To the solution was then added 10 g of 5% palladium carbon. The reaction mixture was then stirred at a hydrogen pressure of 4 kg/cm2 for 6 hours. The catalyst was then removed by filtration. The solvent was then distilled off. The residue was then dissolved in 180 ml of N,N-dimethylformamide. To the solution was then added 18 g of potassium t-butoxide. The reaction mixture was then heated to a temperature of 120° C. with stirring for 1 hour. The reaction solution was then allowed to cool to room temperature. To the reaction solution was then added 70 ml of a 10% hydrochloric acid to cause crystallization. The crystal thus precipitated wax filtered off, washed with water, and then dried under reduced pressure. The crystal was then recrystallized from ethanol to obtain 28.0 g of 2-methoxy-6-(trans-4-propylcyclohexyl)naphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468607B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-8d419faecabc4a078c91ec549419e15d |
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| Source note | uspto-grants-2002_10 |
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