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HRID 511392作成日:2026年10月25日

Acetone → 4-Ethoxycyclohexan-1-one

https://huagongshe.com/reaction/511392

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物8-Ethoxy-1,4-dioxaspiro[4.5]decaneHCID 567358—
溶媒WaterHCID 962—
生成物4-Ethoxycyclohexan-1-oneHCID 546470—

反応条件

温度50 °C

反応手順

A mixture of 8-Ethoxy-1,4-dioxa-spiro[4.5]decane (Compound 166F, 2 gm, 10.7 mmol) and pyridinium p-toluene sulfonate (5.4 gm, 21.5 mmol) was taken up in a 1:1 mixture of acetone and water (150 mL) and stirred at 50° C. overnight. The acetone was subsequently removed under reduced pressure and the aqueous solution was extracted with ethyl acetate. The organic layer was washed with water, dried (Na2SO4), and evaporated to give the crude material which was used in the next step without further purification. Yield: 0.8 gm (53%). 1H NMR (CDCl3, 500 MHz): δ 1.24 (t, J=7.1 Hz, 3H), 1.95 (m, 2H), 2.05 (m, 2H), 2.24 (m, 2H), 2.6 (m, 2H), 3.6 (q, J=7.1 Hz 2H), 3.7 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096624B2
出典データセットuspto-grants-2015_08
ORD IDord-c7cfa3ad87444a74aa346534eacbb44c
出典メモuspto-grants-2015_08