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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Formylethyl)-3-isopropenyl-1-methyl-cyclopent-1-eneHCID 12480720—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product2-(2-Carboxyethyl)-3-isopropenyl-1-methyl-cyclopent-1-eneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031132
Source datasetuspto-grants-1977_06
ORD IDord-67c33b3de6904c79a8dc89b0ce94353d
Source noteuspto-grants-1977_06