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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599202Generated: November 2, 2026

Sulfamic Acid → 4-(2-chloro-4-fluorosulphonyl phenylazo)-N-ethyl-N-benzyl aniline

https://huagongshe.com/reaction/1599202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantN-Ethyl-N-benzylanilineHCID 7098—
ReactantNitrosylsulfuric acidHCID 82157—
Reactant4-Amino-3-chlorobenzenesulfonyl fluorideHCID 282751—
ReactantSodium AcetateHCID 517045—
SolventMethanolHCID 887—
SolventAcetic propionic acidHCID 131720610—
Product4-(2-chloro-4-fluorosulphonyl phenylazo)-N-ethyl-N-benzyl anilineHCID 54116824—

Reaction Conditions

Temperature-5 °C

Reaction Steps

3-Chloro-4-amino benzene sulphonylfluoride (1 part) was stirred in acetic/propionic acid 86/14 vol/vol (15 parts) and cooled to -5° C. Nitrosyl sulphuric acid solution (1.9 parts) was added dropwise then stirred at 0°-5° C. for 2 hours. The diazo solution was then added to a stirred mixture of N-ethyl-N-benzyl aniline (2.0 parts), methanol (50 parts), sulphamic acid (0.5 parts) and sodium acetate (5 parts) with ice/water (100 parts) at 0°-5° C. After stirring under these conditions for 1 hour, the dye was filtered off and washed well with water. The damp solid was slurried in methanol (100 parts) and re-filtered. Dried at 50° C. to yield the product 4-(2-chloro-4-fluorosulphonyl phenylazo)-N-ethyl-N-benzyl aniline (1.5 parts). When applied to polyester materials from an aqueous dispersion the dye gave orange shades. λmax 483 nm

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739299
Source datasetuspto-grants-1998_04
ORD IDord-93752aba1eef4916b6bb765541a6b885
Source noteuspto-grants-1998_04