Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Thiocresol | HCID 7930 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68490534 | HCID 68490534 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68488443 | HCID 68488443 | 56.3% |
Reaction Steps
To a solution of 3-methylthiophenol (0.85 g) in DMF (10 mL) was added 60% sodium hydride (81 mg) under a nitrogen atmosphere under ice-cooling. The mixture was stirred at room temperature for 30 minutes under a nitrogen atmosphere, and then was added dropwise to a solution of N-(4-methylphenyl)-3-(phenylsulfonyl)acrylamide (0.85 g) in DMF (10 mL) under ice-cooling. The mixture was stirred at room temperature for 2 hours, alkalinized by addition of a 1N aqueous sodium hydroxide solution, and then extracted with tert-butyl methyl ether (100 mL). The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain N-(4-methylphenyl)-3-(3-methylphenylthio)acrylamide (0.45 g) as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318981B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-98a76a053b004093a13d692b94cccc68 |
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| Source note | uspto-grants-2012_11 |
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