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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322884Generated: October 30, 2026

Acetone → HCID 86756584, compound

https://huagongshe.com/reaction/322884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium BisulfateHCID 516919—
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantHCID 54532626HCID 54532626—
ProductHCID 86756584HCID 86756584—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl (RS)-4-(2-methylphenyl)-4-[2-methylthio-5-(3-thienylmethoxy)phenoxy]butanoate in acetone (20 mL), at 0° C. is treated dropwise with a solution of potassium peroxymonosulphate (1.01 g of commercial 2KHSO5:KHSO4:K2SO4). The reaction mixture is stirred at 0° C. for 20 minutes, then treated with saturated aqueous sodium bisulphate solution (20 mL), and extracted with dichloromethane (2×50 mL). The combined organic extracts are dried over magnesium sulphate, filtered and concentrated in vacuo, to give ethyl (RS,RS)-4-(2-methylphenyl)-4-[2-methyl-sulphinyl-5-(3-thienylmethoxy)phenoxy)-butanoate (0.75 g) in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211234B1
Source datasetuspto-grants-2001_04
ORD IDord-5253d454b7844fb7b6906111a53f4200
Source noteuspto-grants-2001_04