HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614247Generated: October 30, 2026
Water → 1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene
https://huagongshe.com/reaction/614247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| Reactant | Benzaldehyde, 4-(2-methylpropyl)- | HCID 577537 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene | HCID 54562612 | 87.2% |
Reaction Steps
p-Isobutylbenzaldehyde (486 mg) and 450 mg of formaldehyde dimethyl mercaptal S-oxide were dissolved in 1 ml of t-butanol, and 2.0 ml of a 0.608N t-butanol solution of potassium t-butoxide was added. The mixture was stirred at room temperature for 12 hours. Water (0.5 ml) and 50 ml of methylene chloride were added to the reaction mixture. The resulting mixture was dried over anhydrous sodium sulfate. The drying agent and the insoluble matter were removed by filtration, and the filtrate was concentrated under reduced pressure. The oily residue was chromatographed on a silica gel column using methylene chloride as an eluant to afford 701 mg of 1-methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene in a yield of 87%. Samples for analysis were obtained by simple distillation of this product (at a bath temperature of 160° to 170° C./0.02 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04144248 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-7b4a58ef82c649e5ab1840a140114152 |
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| Source note | uspto-grants-1979_03 |
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