戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 437382作成日:2026年10月26日

Sodium Iodide → HCID 13239620、化合物

https://huagongshe.com/reaction/437382

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物4-ChlorobutyrophenoneHCID 253533—
反応物rel-(2R,6S)-2,6-DimethylpiperidineHCID 641768—
生成物HCID 13239620HCID 13239620—

反応手順

A mixture of 619 g. of γ-Chlorobutyrophenone, ethylene ketal, 700 g. of cis-2,6-dimethylpiperidine and 16 g. of sodium iodide is stirred and heated at reflux for 48 hours. The mixture is cooled, diluted with 1 l. of anhydrous ether and filtered to remove cis-2,6-dimethylpiperidine hydrochloride. The filter cake is washed with 1 l. of ether and the filtrate and washings combined. The resulting ether solution is washed five times with 500 ml. portions of water, then extracted with a solution of 300 ml. of concentrated hydrochloric acid in 3 l. of water. The acid extract is washed with 500 ml. of ether, then heated to 70°-80° and allowed to cool to room temperature over a period of 16 hours. The resulting solution is basified with 50% aqueous sodium hydroxide and the organic layer is separated. The aqueous layer is extracted with 500 ml. of ether and the extract is combined with the organic layer. The combined extract is washed several times with water, dried and evaporated. The oily residue is distilled at reduced pressure to give cis-γ-(2,6-dimethylpiperidino)butyrophenone; b.p. 138°-141° C./0.1 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04031101
出典データセットuspto-grants-1977_06
ORD IDord-cf952834d21840f5b0184b6f2c8b8296
出典メモuspto-grants-1977_06