HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (4-Bromophenyl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | 4-(4-Chlorobenzoyl)piperidine hydrochloride | HCID 2777114 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4-Bromophenyl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone | HCID 58484497 | 99.3% |
Reaction Steps
To tetrahydrofuran (120 mL) were added 4-bromobenzoyl chloride (25 g), (4-chlorophenyl)piperidin-4-ylmethanone hydrochloride (30 g) and 1N aqueous sodium hydroxide solution (250 mL), and the mixture was stirred at room temperature for 3 hr. Ethyl acetate was added for partitioning, the organic layer was washed with saturated brine, and the solvent was evaporated. The residue was recrystallized to give the title compound (46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354401B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-c3cefcdddfc7477a9c5dc6cf4f6ff73d |
| Source note | uspto-grants-2013_01 |