HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-[4-(2-Naphthylsulfonyl)piperazinyl]-2-phenoxyethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenoxyacetyl chloride | HCID 69703 | — |
| Reactant | 1-(Naphthalene-2-sulfonyl)piperazine hydrochloride | HCID 22721815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(2-Naphthylsulfonyl)piperazinyl]-2-phenoxyethan-1-one | HCID 1151516 | 76.33% |
Reaction Steps
In a two neck round bottom flask, 1-(naphthalene-2-yl-sulfonyl)piperazine hydrochloride (compound 4, 0.639 moles, 0.200 g) and 2-phenoxyacetylchloride (0.639 moles, 0.109 g) were charged in DCM (20 mL). TEA (2.557 moles, 0.258 g) was added slowly to the reaction flask. The resulting mixture was stirred for 3 h at room temperature. After completion of the reaction, water (10 mL) was added and extracted with DCM (2×20 mL). The combined organic layers were washed with brine (1×20 mL), dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by column chromatography (Silica gel 60-120, 4:6, Ethyl acetate/Hexane) to obtain the title compound (0.200 g, 76.33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115086B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9ba601d60c124c04a9cc67d75af81fd7 |
| Source note | uspto-grants-2015_08 |