HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437482Generated: October 25, 2026
2-Methoxypropene → 4-(5-Isopropenyl-2-methyl-1-cyclopenten-1-yl)-2-butanone
https://huagongshe.com/reaction/437482
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxypropene | HCID 8300 | — |
| Reactant | 3-Isopropenyl-1-methyl-2-methylenecyclopentan-1-ol | HCID 3016494 | — |
| Catalyst | Phosphoric Acid | HCID 1004 | — |
| Product | 4-(5-Isopropenyl-2-methyl-1-cyclopenten-1-yl)-2-butanone | HCID 3775692 | 60.4% |
Reaction Steps
15 drops of 85% phosphoric acid were added to a mixture, cooled in a laboratory autoclave, of 76 g of 3-isopropenyl-1-methyl-2-methylene-cyclopentan-1-ol and 120 g of isopropenyl methyl ether. After gassing with nitrogen, the autoclave was brought, in an oil bath of 180° C, to an internal temperature of 150° C and held at this temperture until a distinct drop in pressure occurred (about 50-75 minutes). The reaction mixture was quenched by intensive cooling, treated with solid potassium hydroxide and concentrated under reduced pressure on a rotary evaporator. By fractional distillation over solid potassium hydroxide there were obtained 58 g (60%) of 3-isopropenyl-1-methyl-2-(3-oxobutyl)-cyclopent-1-ene; boiling point 0.01 = 69°-72° C; nD20 = 1.4836. The compound has a woody, camphoraceous, ionone-like fragrance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04031132 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-047948aa7aa94d1389a8a08a24c3a8c0 |
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| Source note | uspto-grants-1977_06 |
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