Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | HCID 54532626 | HCID 54532626 | — |
| Product | HCID 86756584 | HCID 86756584 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211234B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-5253d454b7844fb7b6906111a53f4200 |
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| Source note | uspto-grants-2001_04 |
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