HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082870Generated: October 31, 2026
Water → 3-Amino-5-(hydroxymethyl)-2-phenoxybenzene-1-sulfonamide
https://huagongshe.com/reaction/2082870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 3-amino-4-phenoxy-5-sulfamoylbenzoate | HCID 20294607 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Amino-5-(hydroxymethyl)-2-phenoxybenzene-1-sulfonamide | HCID 54036191 | — |
Reaction Steps
To a stirred mixture of lithium aluminium hydride (12.5 g) and dry dioxane (250 ml), a solution of ethyl 3-amino-4-phenoxy-5-sulfamylbenzoate (50 g) in dry dioxane (250 ml) is dropwise added at 90° C during about one hour. After additonal stirring and heating for 3 hours the mixture is cooled, and ethyl acetate (25 ml) followed by water (50 ml) and 4 N acetic acid (310 ml) are very cautiously added dropwise. The solvents are thereafter removed in vacuo, and the residue is extracted with ethyl acetate (1 liter). The insoluble inorganic material is removed by filtration, and the filtrate is washed with aqueous sodium hydrogen carbonate and with water, and is then dried in the presence of magnesium sulphate. After filtration, the solvent is removed in vacuo to yield crude 3-amino-4-phenoxy-5-sulfamylbenzyl alcohol. After recrystallization from aqueous ethanol it is obtained with a melting point of 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04082851 |
|---|
| Source dataset | uspto-grants-1978_04 |
|---|
| ORD ID | ord-2ca56cadb9064ea5a99aad3bdb7da680 |
|---|
| Source note | uspto-grants-1978_04 |
|---|