HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869371Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 17989157, compound
https://huagongshe.com/reaction/1869371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(2,5-Difluorophenyl)-4-methyl-2-(trifluoromethyl)pentane-1,2-diol | HCID 17989169 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 17989157 | HCID 17989157 | 85.6% |
Reaction Steps
800 mg (2.8 mmol) of 4-(2,5-difluorophenyl)-4-methyl-2-trifluoromethyl-pentane-1,2-diol is introduced into 20 ml of dichloromethane, and at 0° C., 9.5 ml of DMSO and 1.95 ml of triethylamine are added. The solution is slowly mixed with 1.34 g (8.4 mmol) of SO3-pyridine complex, and it is stirred for 2 hours at 0° C. The mixture is dispersed between saturated ammonium chloride solution and MTBE, the phases are separated, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with water and saturated NaCl solution and dried with NaSO4. It is concentrated by evaporation and chromatographed on silica gel with hexane/ethyl acetate (30%). 710 mg of the desired product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638515B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-21f3a06b0c284c378d69c46ea5c9436e |
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| Source note | uspto-grants-2009_12 |
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