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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599203Generated: October 25, 2026

Sulfamic Acid → 4-(2-methoxy-5-fluorosulphonylphenylazo)-3-methyl-N-ethyl-N-benzyl aniline

https://huagongshe.com/reaction/1599203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantN-Benzyl-N-ethyl-m-toluidineHCID 67076—
ReactantNitrosylsulfuric acidHCID 82157—
Reactant3-Amino-4-methoxyphenylsulphonyl fluorideHCID 96952—
ReactantSodium AcetateHCID 517045—
SolventMethanolHCID 887—
SolventAcetic propionic acidHCID 131720610—
Product4-(2-methoxy-5-fluorosulphonylphenylazo)-3-methyl-N-ethyl-N-benzyl anilineHCID 18930927—

Reaction Steps

3-Amino-4-methoxy benzene sulphonylfluoride (1 part) was stirred in acetic/propionic acid 86/14 vol/vol (15 parts) and cooled to 0°-5° C. Nitrosyl sulphuric acid solution (1.9 parts) was dropwise and stirred at 0°-5° C. for 2 hours. The diazo solution was then added to a stirred mixture of N-ethyl-N-benzyl-m-toluidine (1.3 parts), methanol (50 parts), sulphamic acid (0.5 parts) and sodium acetate (5 parts) stirring in ice/water at 0°-5° C. After stirring for 2 hours under these conditions, the dye was filtered off and washed well with water. The damp solid was slurried in water and re-filtered. The dye was then stirred in methanol at room temperature for 1 hour, filtered, and dried at 50° C. to yield the product, 4-(2-methoxy-5-fluorosulphonylphenylazo)-3-methyl-N-ethyl-N-benzyl aniline (1.5 parts). When applied to polyester materials from an aqueous dispersion, the dye gave yellow shades. λmax 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739299
Source datasetuspto-grants-1998_04
ORD IDord-d2e18ef566134b22ac2f490a0fb220e5
Source noteuspto-grants-1998_04