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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834089Generated: October 30, 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/1834089

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 numberUS04068084
Source datasetuspto-grants-1978_01
ORD IDord-487585eb39a14e6a90c8121d48caff37
Source noteuspto-grants-1978_01