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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658179Generated: October 26, 2026

Ethyl 1-propenyl ether → 2-(2-Formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-ene

https://huagongshe.com/reaction/1658179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-propenyl etherHCID 13570—
Reactant3-Isopropenyl-1-methyl-2-methylenecyclopentan-1-olHCID 3016494—
CatalystPhosphoric AcidHCID 1004—
Product2-(2-Formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-eneHCID 2138852967%

Reaction Steps

15 drops of 85% phosphoric acid were added to a mixture, cooled to -30°C in a laboratory autoclave, of 76 g of 3-isopropenyl-1-methyl-2-methylene-cyclopentan-1-ol and 130 g of ethyl 1-propenyl ether. After gassing with nitrogen, the autoclave was brought, in an oil bath of 180°C, to an internal temperature of 150°C (this took about 15 minutes) and held at this temperature until a distinct drop in pressure occurred (about 75 minutes). The reaction mixture was then quenched, taken up in ether, washed with aqueous bicarbonate solution and water, the solution dried over anhydrous magnesium sulphate and concentrated under reduced pressure. The crude product (135 g), obtained as a yellow oil, was fractionated and yielded 64 g (67%) of pure 2-(2-formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-ene having woody, earthy, musty fragrance; boiling point 0.005 = 51°C; nD20 = 1.4825; IRfilm : μmax = 3090, 2730, 1735, 1645, 1460, 1380 and 898 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963675
Source datasetuspto-grants-1976_06
ORD IDord-d3355d8304584aa2a4c043c278cff25c
Source noteuspto-grants-1976_06