HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-5-ethanesulfonyl-thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | 2-Bromo-5-(ethylthio)thiophene | HCID 22032079 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-5-ethanesulfonyl-thiophene | HCID 59264658 | — |
Reaction Steps
A 25 mL THF/MeOH (2:1) solution of 2-Bromo-5-ethylsulfanyl-thiophene (CAS 19991-60-7) is stirred at 0-10° C. while 8 mL H2O, then 3 equivalents of Oxone are added. The reaction mixture is stirred three hours at room temperature, then is diluted with CH2Cl2, filtered, washed with aq. NaHCO3 and brine, dried (Na2SO4) and concentrated in vacuo. The crude mixture is purified by silica gel column chromatography (gradient: 0-20% EtOAc/CH2Cl2) to give title intermediate that is confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705025B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-d1cabdcb221448c2bb76422091dc66d2 |
| Source note | uspto-grants-2010_04 |