HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388539Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 12815947, compound
https://huagongshe.com/reaction/1388539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 12815944 | HCID 12815944 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12815947 | HCID 12815947 | 77.7% |
Reaction Steps
A mixture of 55.7 g of crude 2-chloromethyl-4-(trifluoromethylthio)chlorobenzene, 23 g of potassium acetate, 150 ml of dimethyl sulfoxide and 10 g of triethylbenzylammonium chloride is stirred for 5 hours at 60° C. It is decomposed by pouring into water, extracted with benzene and the benzene evaporated. The oily residue is dissolved in 200 ml of ethanol, 100 ml of water and 20 ml of hydrochloric acid are added and the mixture is stirred and refluxed for 7 hours. Ethanol is distilled off, the residue mixed with water and extracted with benzene. The oil obtained by evaporation of the dried extract, is distilled in vacuo. There are obtained 40.2 g crude 2-chloro-5-(trifluoromethylthio)benzyl alcohol boiling at 140°-150° C./2 kPa. According to the 1H-NMR spectrum the product contains approximately 80% of the named compound and the remainder is the position isomer. In this state the substance is suitable for further processing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431808 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-850dc277fe464c80af6cdc1cd06e7244 |
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| Source note | uspto-grants-1984_02 |
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