HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl(6-((2,4-dichlorobenzyl)sulfinyl)-1-benzothiophen-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Ethyl(6-((2,4-dichlorobenzyl)sulfanyl)-1-benzothiophen-3-yl)acetate | HCID 118667019 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl(6-((2,4-dichlorobenzyl)sulfinyl)-1-benzothiophen-3-yl)acetate | HCID 118667020 | — |
Reaction Steps
To a mixture of ethyl(6-((2,4-dichlorobenzyl)sulfanyl)-1-benzothiophen-3-yl)acetate (315 mg), water (3.00 mL) and CH3CN (3.00 mL) was added NaIO4 (164 mg) at room temperature. The mixture was stirred at room temperature for 1 day. To the mixture was added NaIO4 (164 mg), and the mixture was stirred for further 1 day. To the mixture was added saturated aqueous Na2S2O3 at room temperature, and the mixture was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (204 mg). The residue was recrystallized from EtOAc-hexane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238639B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-998e3555062b434c886255604138adbe |
| Source note | uspto-grants-2016_01 |