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HRID 1599201생성일: 2026년 10월 26일

Sulfamic Acid → 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline

https://huagongshe.com/reaction/1599201

반응식

참여 물질

역할이름HCID투입량
반응물Sulfamic AcidHCID 5987—
반응물N-Ethyl-N-benzylanilineHCID 7098—
반응물Nitrosylsulfuric acidHCID 82157—
반응물3-Amino-4-chlorobenzenesulphonyl fluorideHCID 97383—
용매MethanolHCID 887—
용매Acetic propionic acidHCID 131720610—
생성물4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl anilineHCID 53969731—

반응 단계

3-Amino-4-chloro benzene sulphonyl fluoride (2 parts) was stirred in acetic/propionic acid 86/14 vol/vol (25 parts) and cooled to 0°-5° C. Nitrosyl sulphuric acid solution (3.8 parts) was added dropwise at 0°-5° C. and stirred under these conditions for 2 hours. The diazo solution was then added to a mixture of N-ethyl-N-benzyl aniline (2.7 parts), methanol (100 parts) and sulphamic acid (1 part) stirring at 0°-5° C. After stirring under these conditions for 30 mins, ice/water (100 parts) was added and the mixture stirred for a further 1 hour. The product was isolated by filtration, washed with water and pulled dry. The damp solid was then slurried in methanol (100 parts) and refiltered. Dried at 50° C. to yield 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline (2.3 parts).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05739299
출처 데이터셋uspto-grants-1998_04
ORD IDord-559d64b2333f46a0803664a50d614084
출처 메모uspto-grants-1998_04