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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591488Generated: November 1, 2026

Water → Ethyl(6-((2,4-dichlorobenzyl)sulfinyl)-1-benzothiophen-3-yl)acetate

https://huagongshe.com/reaction/591488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ThiosulfateHCID 24477—
ReactantEthyl(6-((2,4-dichlorobenzyl)sulfanyl)-1-benzothiophen-3-yl)acetateHCID 118667019—
SolventAcetonitrileHCID 6342—
ProductEthyl(6-((2,4-dichlorobenzyl)sulfinyl)-1-benzothiophen-3-yl)acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-998e3555062b434c886255604138adbe
Source noteuspto-grants-2016_01