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HRID 34971作成日:2026年10月24日

5-Bromopentanenitrile → 4-(2-Propyl-3-chlorophenoxy)butane nitrile

https://huagongshe.com/ja/reaction/34971

反応式

関与物質

役割名称HCID仕込み量
反応物5-BromopentanenitrileHCID 79435—
反応物2-Propyl3-chlorophenolHCID 15747295—
生成物4-(2-Propyl-3-chlorophenoxy)butane nitrileHCID 21297257—

反応手順

Five and seven-tenths grams of 2-propyl3-chlorophenol were then reacted with 5.9 ml. of 5bromovaleronitrile following the procedure of Example 2A. The resulting 4-(2-propyl-3-chlorophenoxy)butane nitrile was provided by chromatography. This purified nitrile intermediate (3.3 g.) was dissolved in about 65 ml. of methylene chloride to which 3.0 g. of aluminum chloride and 1.7 ml. of acetyl chloride had been added and the reaction was heated to reflux overnight. The reaction was cooled, additional methylene chloride was added, and the mixture was poured into ice/hydrochloric acid. The layers were separated and the organic layer was washed first with an aqueous sodium bicarbonate solution and then with water. The organic solution was dried over sodium sulfate and evaporated to dryness. Purification by chromatography provided 2.67 g. of the desired 4-(2-propyl-3-chloro4-acetylphenoxy)butane nitrile. NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764521
出典データセットuspto-grants-1988_08
ORD IDord-f52101a2e8e040ccb3b160f565907bd0
出典メモuspto-grants-1988_08