HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 4-(4-hydroxyphenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(1-Piperazinyl)phenol | HCID 92467 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 4-(4-hydroxyphenyl)piperazine-1-carboxylate | HCID 54123735 | 69.4% |
Reaction Steps
To a suspension of 1-(4-hydroxyphenyl)piperazine (50 g) and potassium carbonate (46.5 g) in N,N-dimethylformamide (100 ml) was added dropwise benzyl chloroformate (47.86 g) at 0 to 10° C., and stirred for 4 hours at ambient temperature. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure. The residue was chromatographed on a column of silica gel eluting with dichloromethane/methyl alcohol (30:1) to give 4-(4-hydroxyphenyl)piperazine-1-carboxylic acid benzyl ester (60.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884868B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-6071c79913c64d0a9b3d1c4286c85368 |
| Source note | uspto-grants-2005_04 |