HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437486Generated: October 26, 2026
2-(2-Formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene → 2-(2-Carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene
https://huagongshe.com/reaction/437486
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(2-Formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene | HCID 12480720 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene | HCID 21388533 | — |
Reaction Steps
A solution of 25 g of 2-(2-formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene in 1200 ml of acetone was treated at -10° C with 55 ml of Jones reagent. The resulting brown mixture was poured on to ice/sodium bicarbonate solution. Ether extraction, washing neutral with sodium bicarbonate solution, saturated sodium chloride solution and water, drying of the extract with magnesium sulphate and removal of the solvent under reduced pressure yielded 20 g (80%) of a weakly yellow oily crude product from which there were obtained by distillation 15 g of pure 2-(2-carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-ene; boiling point 0.01 = 102° C; IRfilm : νmax = 3600-2400, 1720, 1645, 1450, 1420, 1380, 1330, 1290, 1220, 1085, 945 and 900 cm-1. The compound has a woody, spicy, weakly sweetish and somewhat musty 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-67c33b3de6904c79a8dc89b0ce94353d |
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| Source note | uspto-grants-1977_06 |
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