Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | HCID 23618803 | HCID 23618803 | — |
| Reactant | 7-((3-(4-Acetyl-3-hydroxy-2-propylphenoxy)-2-hydroxypropoxyl))-4-oxo-8-propyl-4H-chromene-2-carboxy late, sodium salt | HCID 23662025 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 20289615 | HCID 20289615 | — |
Reaction Steps
Dissolve 10.9 gm of 7-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)-2-hydroxypropoxy]-4-oxo-8-propyl-4H-1-benzopyran-2-carboxylic acid sodium salt in 250 ml of 28% ammonium hydroxide solution. Cool the mixture in an ice-water bath. Add 285 ml of a 0.2 m aqueous potassium triiodide solution dropwise. Stir in the cold for 15 minutes. Add sodium bisulfite until iodine color is discharged. Acidify the mixture slowly with 20% aqueous hydrochloric acid. Separate the solids by filtration, wash with water and dry. Dissolve the solids in methanol and esterify with diazomethane in ether. Chromatograph on silica gel, eluting with 15% ethyl acetate in toluene (mp 137°-141° C.). Crystallize from toluene (mp 150°-153° C.). Reflux 2.1 gm of ester product in a mixture of 2.1 gm of sodium bicarbonate, 200 ml of denatured alcohol and 20 ml of water for 1 hour. Strip the mixture to dryness and triturate the residue in ethyl acetate. Separate the solids, dissolve in water and acidify with 10% aqueous hydrochloric acid. Separate the solids by filtration. (mp 179°-182° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04252818 |
|---|
| Source dataset | uspto-grants-1981_02 |
|---|
| ORD ID | ord-17bcc1be1d6d4d0282342732ba8fa521 |
|---|
| Source note | uspto-grants-1981_02 |
|---|