HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetate → Methyl 4-(4-cyanophenyl)-1-piperazineacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetate | HCID 6226 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Piperazin-1-yl)benzonitrile | HCID 2733995 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-(4-cyanophenyl)-1-piperazineacetate | HCID 19391362 | — |
Reaction Steps
2 g of 1-(4-cyanophenyl)-piperazine are stirred in 20 ml of dry dimethylformamide at ambient temperature with 0.51 g of a 50% sodium hydride/oil suspension. Whilst cooling in a water bath, 1 ml of bromoacetate is added. Then the mixture is diluted with water and extracted with ethyl acetate. The combined ethyl acetate extracts are dried and the solvent is removed under reduced pressure. The residue remaining is chromatographed with methylene chloride/methanol (98:2) over silica gel. The product is triturated with ether, suction filtered and washed with petroleum ether. Yield: 1.6 g (58% of theory), Melting point: 92°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05442064 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-be70ac56f8c249ba97ef284b4b1414fc |
| Source note | uspto-grants-1995_08 |