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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | N-Ethyl-N-benzylaniline | HCID 7098 | — |
| Reactant | Nitrosylsulfuric acid | HCID 82157 | — |
| Reactant | 4-Amino-3-chlorobenzenesulfonyl fluoride | HCID 282751 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetic propionic acid | HCID 131720610 | — |
| Product | 4-(2-chloro-4-fluorosulphonyl phenylazo)-N-ethyl-N-benzyl aniline | HCID 54116824 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739299 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-93752aba1eef4916b6bb765541a6b885 |
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| Source note | uspto-grants-1998_04 |
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