Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mandelic Acid | HCID 1292 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 12440727 | HCID 12440727 | — |
Reaction Steps
4.56 g (30 mM) of DL-mandelic acid are dissolved in 100 ml. of carbon disulfide and 3.37 g. (60 mM) of pulverized potassium hydroxide are added all at once. Absolute dimethylsulfoxide is then added with stirring until a clear solution is obtained. The whole is stirred for 1 hour and then 4.26 g (30 mM) of methyl iodide are added. After 4 hours the carbon disulfide is removed in vacuum and the oily residue is dissolved in 200 ml. of water. The aqueous solution is extracted three times with 50 ml. of ether. After cooling the aqueous phase to 5°, it is acidified with 2N hydrochloric acid and extracted with ether. From the ether, 3.1 g. of crude DL-α-[(methylthio)thioxomethoxy]benzene acetic acid is obtained. Recrystallization from benzol/cyclohexane yields 2.7 g., m.p. 109°-110°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943130 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-deb42e8ba60848b3966bb011d9d61336 |
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| Source note | uspto-grants-1976_03 |
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