Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methane, chloro(methylsulfinyl)- | HCID 151872 | — |
| Product | HCID 12522571 | HCID 12522571 | 87.6% |
Reaction Steps
Potassium hydroxide (460 mg) was added in an atmosphere of nitrogen to a mixture of 560 mg of chloromethyl methyl sulfoxide and 616 mg of thiophenol, and then the mixture was heated at 60° C. for 13.5 hours. With addition of 3 ml. of water, the mixture was extracted with chloroform. The extract was dried using anhydrous sodium sulfate, and then subjected to column-chromatography [silica gel, chloroform-ethyl acetate (9:1 )] to yield 812 mg of methyl phenylthiomethyl sulfoxide having a boiling point of 148° C./0.5 mmHg and an nD25 of 1.6053 as a colorless liquid in a yield of 87.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029712 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-8319681a216d471c9c6dd0b6c65f7633 |
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| Source note | uspto-grants-1977_06 |
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