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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1939853생성일: 2026년 10월 26일

4,4-Diethoxybutylamine → N-(4,4-diethoxybutyl)benzenesulfonamide

https://huagongshe.com/reaction/1939853

반응식

참여 물질

역할이름HCID투입량
반응물4,4-DiethoxybutylamineHCID 80672—
반응물Benzene sulphochlorideHCID 22564087—
생성물N-(4,4-diethoxybutyl)benzenesulfonamideHCID 7027054886%

반응 단계

42 g 4-amino butyraldehyde diethyl acetal and 88 g benzene sulfochloride are processed as explained in Preparation Example 1. The reaction mixture is not clear from the very beginning and vigorous stirring is therefore indispensable. Methylene chloride is used for the extraction of the sulfonamide acetal. Yield: 86% based on the amino acetal used. The product will crystallize when standing for an extended time at room temperature; melting point: 109°-111°° C.; for further purification recrystallization from a 2:1 volume mixture of water and ethanol is possible.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05698360
출처 데이터셋uspto-grants-1997_12
ORD IDord-f479b9f1c492412d8f65bb6cdc580c4f
출처 메모uspto-grants-1997_12