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HRID 437488作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/437488

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 1-propenyl etherHCID 13570—
反応物3-Isopropenyl-1-methyl-2-methylenecyclopentan-1-olHCID 3016494—
触媒Phosphoric AcidHCID 1004—
生成物2-(2-Formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-eneHCID 2138852967%

反応手順

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 : νmax = 3090, 2730, 1735, 1645, 1460, 1380 and 898 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04031132
出典データセットuspto-grants-1977_06
ORD IDord-2ff6b67204be465e9b852afb903a1b4b
出典メモuspto-grants-1977_06