HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(Benzyloxycarbonylamino)-2-phenylethyl-phosphonic acid
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 | 1-Benzyloxycarbonylamino-2-phenylethylphosphonous acid | HCID 14551341 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Benzyloxycarbonylamino)-2-phenylethyl-phosphonic acid | HCID 10980569 | — |
Reaction Steps
To a solution of 1-benzyloxycarbonylamino2-phenylethyl phosphonous acid (0.5 g, 0.0016 mole) in acetone (20 ml) and water (10 ml) was added a 10% solution of sodium hydroxide in water until a pH of about 7 was reached. A solution of KMnO4 (0.14 g, 0.00086 mole, 0.55 equiv.) 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 white precipitate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670193 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-da1de098c3ae402db57b5e38d1d3a25a |
| Source note | uspto-grants-1987_06 |