HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 8-(2-hydroxyethylsulfamyl)-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-sulfonyl chloride | HCID 19972799 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(2-hydroxyethylsulfamyl)-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran | HCID 19972778 | — |
Reaction Steps
A solution of 5 g of Intermediate VIII in 37 ml of tetrahydrofuran was added dropwise at 0° C. to a mixture of 2.5 ml of ethanolamine and 2.5 ml of triethylamine in 25 ml of tetrahydrofuran. After stirring at 20°-25° C., the reaction mixture was poured into 400 ml of water. A precipitate formed, and was collected by suction filtration, washed with water and air dried, yielding 4.6 g of 8-(2-hydroxyethylsulfamyl)-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran, melting at 186°-187° C. after crystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05605896 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-84b5f9daeb76423eae8d4c0b393cc29b |
| Source note | uspto-grants-1997_02 |