Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Furfurylamine | HCID 3438 | — |
| Reactant | HCID 13333282 | HCID 13333282 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 12274618 | HCID 12274618 | — |
Reaction Steps
43 g (1.0 mol) of the 2,4-diphenoxy-5-sulfamoyl-benzoic acid prepared according to (d) were stirred for 4 hours under nitrogen at 135° C with 90 ml of freshly distilled furfurylamine. The faintly yellow reaction solution, which had been cooled to about 80° C, was then introduced while stirring into 1 l of 10 % acetic acid, and the pH of the mixture was then adjusted to 3 by means of 5N HCl. After standing for a short time at room temperature, the N-(2-furylmethyl)-4-phenoxy-5-sulfamoyl-anthranilic acid which had precipitated in crystals was suction-filtered, washed with water and ethanol and dried on a steam bath.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04001284 |
|---|
| Source dataset | uspto-grants-1977_01 |
|---|
| ORD ID | ord-cfa58202101443c78f6eb848e3419d1f |
|---|
| Source note | uspto-grants-1977_01 |
|---|