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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437382생성일: 2026년 10월 24일

Sodium Iodide → HCID 13239620, 화합물

https://huagongshe.com/ko/reaction/437382

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물4-ChlorobutyrophenoneHCID 253533—
반응물rel-(2R,6S)-2,6-DimethylpiperidineHCID 641768—
생성물HCID 13239620HCID 13239620—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04031101
출처 데이터셋uspto-grants-1977_06
ORD IDord-cf952834d21840f5b0184b6f2c8b8296
출처 메모uspto-grants-1977_06