HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → g-Phenylpropylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Phosphonous acid | HCID 3014827 | — |
| Reactant | 3-Phenylpropyl phosphonous acid | HCID 13945794 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | g-Phenylpropylphosphonate | HCID 15919487 | — |
Reaction Steps
To a solution of 3-phenylpropyl phosphonous acid (0.92 g, 0.005 mole) in acetone (10 ml) and water (10 ml) was added a solution of sodium hydroxide (0.2 g, 0.005 mole) in water (10 ml) until a pH of about 7 was reached. A solution of KMnO4 (0.474 g, 0.003 mole) in water (10 ml) was added slowly to the vigorously stirred solution of phosphonous acid at 20°-25° C. After the addition (5 minutes), the reaction mixture was stirred for 5 minutes at ambient temperature and acidified with concentrated HCl acid until a pH of 1 was reached. Saturated sodium bisulfite solution was added to the reaction mixture thereby resulting in formation of a precipitate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670193 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-4a0a1ce46ac040c3ab115b5c552108e5 |
| Source note | uspto-grants-1987_06 |