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HRID 1646429作成日:2026年10月27日

Ethanol → Ethyl 3-(4-chlorophenyl)-2,2-dimethylpropanoate

https://huagongshe.com/reaction/1646429

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物HexaneHCID 8058—
反応物Hydrofluoric AcidHCID 14917—
反応物Benzenemethanol, 4-chloro-alpha-(1-methylethyl)-HCID 202426—
反応物HCID 178418416HCID 178418416—
触媒Hastelloy CHCID 11332432—
生成物Ethyl 3-(4-chlorophenyl)-2,2-dimethylpropanoateHCID 12373578—

反応条件

温度-30 °C

反応手順

1-(4'-Chlorophenyl)-2-methyl-1-propanol (9.6 grams, 0.05 moles), ethanol (4.5 grams, 0.1 mole), and hexane (32 grams) are charged into a 300 cubic centimeter Hastelloy C autoclave. The autoclave is purged twice with nitrogen, evacuated to 100 mm Hg, and cooled to -30° C. Hydrogen fluoride (75 grams, 3.25 mole) is then added and the reactor is pressurized to 600 psig with carbon monoxide. The reaction mass is stirred for about an hour at room temperature. The hydrogen fluoride is vented and the contents are removed and poured onto crushed ice. A solution of 45% potassium hydroxide is added to the mixture until the pH of the mixture is adjusted to 6.0-6.5. The mixture is then extracted with ethyl acetate (3 times with 150 ml of ethyl acetate each time). The combined organic extract is dried with anhydrous magnesium sulfate, filtered, and concentrated to yield the crude product. The crude product is distilled under vacuum to give pure ethyl 2,2-dimethyl-3-(4'-chlorophenyl)propanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05179229
出典データセットuspto-grants-1993_01
ORD IDord-4b0dbf58f1b3417681ace3e3d80539f9
出典メモuspto-grants-1993_01