HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54345800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 53755237 | HCID 53755237 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54345800 | HCID 54345800 | — |
Reaction Steps
30 g. of ethyl 4-amino-3-p-chlorophenyl-2-phenyl-butyrate are heated for 15 minutes at 150°C. Liberation of ethanol is observed. The reaction medium is taken up in 120 ml. of toluene and the resulting solution is filered. After cooling the solution, the crystals formed are separated and recrystallized several times from toluene. 12 g. of 4-p-chlorophenyl-3-phenyl-2-pyrrolidinone are obtained; m.p. 148°-151°C. Nuclear magnetic resonance analysis shows that it is the cis-isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03956314 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-073811f1b1b04b0b8c2bb77d1e7c3aa0 |
| Source note | uspto-grants-1976_05 |