HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → methyl P-methyl-2-nitro-5-phenylthiophenylphosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl P-methyl-2-nitro-5-chlorophenylphosphinate | HCID 53860251 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl P-methyl-2-nitro-5-phenylthiophenylphosphinate | HCID 54434247 | — |
Reaction Steps
To a mixture of ethyl P-methyl-2-nitro-5-chlorophenylphosphinate (20.0 mmol) and thiophenol (40.0 mmol) in 20 ml of ethanol is added sodium hydroxide (60.0 mmol) in 1 ml of water. The mixture is heated under reflux for 24 hours. The reaction mixture is poured into water, acidified with dilute HCl and extracted with methylene chloride (2×). The combined extracts are washed with brine, dried and evaporated to dryness. The resulting oily residue is treated with diazomethane in methanol, concentrated and purified by preparative TLC to yield methyl P-methyl-2-nitro-5-phenylthiophenylphosphinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04520197 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-9be7aedd1afd4fbb8d7420ed4e565160 |
| Source note | uspto-grants-1985_05 |