HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-[(4-Fluorophenyl)thio]-2-hydroxy-2-methylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorothiophenol | HCID 67789 | — |
| Reactant | Methyl 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionate | HCID 21966928 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[(4-Fluorophenyl)thio]-2-hydroxy-2-methylpropanoic acid | HCID 9813367 | — |
Reaction Steps
The methyl 2-methyl-oxirane-carboxylate of formula (1), which was obtained by epoxidation, was reacted with 4-fluorothiophenol [formula (2)] in the presence of sodium hydride under the conditions listed in Scheme-2. The obtained methyl 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionate of formula (3) was hydrolyzed with potassium hydroxide in aqueous ethanol over a period of 22 hours to yield the 2-hydroxy-2-methyl-3-(4-fluorophenylthio)-propionic acid of formula (4), which was converted into the acid chloride of formula (5) with thionyl chloride in dimethyl acetamide at −15° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06797843B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-d1428382e5594bee98432940656e5c4c |
| Source note | uspto-grants-2004_09 |