HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 19595593, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 9824895 | HCID 9824895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19595593 | HCID 19595593 | 78.4% |
Reaction Steps
1 g (0.0022 mole) of (Z)-2-[3-[1-(4-chlorophenyl)-1-[4-(methylsulphonyl)phenyl]methylene]-2-oxo-pyrrolidin-1-yl]ethyl acetate are placed in solution in a mixture of 13 ml of ethanol and 11 ml of water and treated with 0.1 g (1.1 eq.) of sodium hydroxide. The medium is stirred at ambient temperature for 4 h, then the ethanol is evaporated off. The aqueous phase is extracted with dichloromethane. The organic phase is washed with water, dried and concentrated. The residue is taken up into t-butyl methyl ether. 0.7 g of (Z)-3-[1-(4-chlorophenyl)-1-[4-(methylsulphonyl)phenyl]methylene]-1-(2-hydroxyethyl)-pyrrolidin-2-one are thus obtained as a yellow solid of melting point 187-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06004994 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-794833f1f50f40afa88cdfb983813347 |
| Source note | uspto-grants-1999_12 |