HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252890Generated: October 23, 2026
Phosphoric Acid → 3-{Ethyl-[4-(5-nitro-benzo[c]isothiazol-3-ylazo)-phenyl]-amino}-propionic acid vinyl ester
https://huagongshe.com/en/reaction/252890
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Nitrosylsulfuric acid | HCID 82157 | — |
| Reactant | 7-Amino-5-nitrobenzisothiazole | HCID 20038975 | — |
| Reactant | 3-(Ethyl-phenyl-amino)-propionic acid vinyl ester | HCID 67266914 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-{Ethyl-[4-(5-nitro-benzo[c]isothiazol-3-ylazo)-phenyl]-amino}-propionic acid vinyl ester | HCID 59141511 | — |
Reaction Steps
5.9 parts of 7-amino-5-nitrobenzisothiazole, 30 parts of 98% sulfuric acid and 8 parts of 85% phosphoric acid were charged, heated at 60° C. for 30 mins, then cooled to 5° C. 11.4 parts of 40% (w/w) nitrosyl sulfuric acid were added, whilst the temperature was held below 10° C. The diazotization mixture was stirred for a further 2 hrs at 5-10° C. To a separate vessel were charged 6.5 parts of 3-(ethyl-phenyl-amino)-propionic acid vinyl ester, 100 parts of methanol, 1 part sulfamic acid and 100 parts of ice. With stirring, the diazotization mixture was slowly added followed by a further 300 parts of ice. The reaction mixture was stirred over night and the product was isolated by filtration, washed with water and dried to yield 10.1 parts of 3-{ethyl-[4-(5-nitro-benzo[c]isothiazol-3-ylazo)-phenyl]-amino}-propionic acid vinyl ester. λmax=606 nm (DMF).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07871446B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a91548c9c95d4b949953dc810420b30e |
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| Source note | uspto-grants-2011_01 |
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