HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 4-((Benzyloxy)carbonyl)piperazine-2-carboxylic acid | HCID 5058362 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acid | HCID 12109643 | — |
Reaction Steps
A mixture of 12.0 g. (0.04 mole) of 4-carbobenzoxypiperazine-2-carboxylic acid, 8.4 g. (0.06 mole) of o-nitrofluorobenzene, 16 g. of triethylamine and 100 ml. of dimethylsulfoxide is heated at 90° for 8 1/2 hours, cooled, diluted with water (300 ml.) and extracted with ether. The aqueous phase is then acidified with dilute hydrochloric acid and extracted with ether. The combined ether extracts are diluted with 1/3 its volume of pentane. The ether-pentane solution is washed with water, dried (MgSO4) and concentrated to give 14 g. of yellow-orange glassy product. Thin layer chromatrgraphy analysis (1% acetic acid in benzene on a silica gel plate) shows 1 main spot with a faint second impurity spot.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089958 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-a0edf31317c248e5b4191da6c11de254 |
| Source note | uspto-grants-1978_05 |