Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 10437294 | HCID 10437294 | — |
| Product | HCID 10324587 | HCID 10324587 | — |
Reaction Steps
{4-[3,3-Bis-(3-trifluoromethyl-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester (100 mg, 0.23 mmol) was dissolved in ethanol (10 ml).1N NaOH (3 ml, 3 mmol) was added at room temperature and the reaction mixture was stirred for 18 h at 5° C. after which it was treated with 1N HCl (3 ml) and extracted with dichloromethane (2×20 ml). The combined organic phases were dried and evapotated to give the title compound in 20 mg (5%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129268B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-0e141c83e62a4f31a530e71b880fc462 |
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| Source note | uspto-grants-2006_10 |
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