HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → HCID 66584943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 66584760 | HCID 66584760 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66584943 | HCID 66584943 | 33.4% |
Reaction Steps
To a solution of 38.3 g (164 mmol) of ethyl 4-(3-fluoro-phenyl)-1H-pyrrole-3-carboxylate in 380 ml of tetrahydrofuran are added, over 30 minutes, 32.1 g (181 mmol) of N-bromosuccinimide (CAS 128-08-5), and the mixture is then stirred for 3 hours at reflux. After cooling, 200 ml of aqueous 5% sodium thiosulfate solution are added and the reaction product is extracted with ethyl acetate. The organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure, to give 17.1 g of ethyl 5-bromo-4-(3-fluorophenyl)-1H-pyrrole-3-carboxylate in the form of a white powder after recrystallizing from diisopropyl ether, filtering off and drying.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08791119B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-feeeaf794f754a9db44771be381c8adc |
| Source note | uspto-grants-2014_07 |