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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1599201Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1599201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfamic AcidHCID 5987—
EduktN-Ethyl-N-benzylanilineHCID 7098—
EduktNitrosylsulfuric acidHCID 82157—
Edukt3-Amino-4-chlorobenzenesulphonyl fluorideHCID 97383—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetic propionic acidHCID 131720610—
Produkt4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl anilineHCID 53969731—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05739299
Quelldatensatzuspto-grants-1998_04
ORD IDord-559d64b2333f46a0803664a50d614084
Quellennotizuspto-grants-1998_04