HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442923Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 57022280, compound
https://huagongshe.com/reaction/442923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57049612 | HCID 57049612 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57022280 | HCID 57022280 | 80% |
Reaction Steps
Sulfur trioxide pyridine complex (720 mg, 4.5 mmol) was added to a solution of 3-[3-(benzo-2,1,3-thiadiazole-4-sulfonyloxy)-5-methylphenoxy]propanol (565 mg, 1.5 mmol), as prepared in the preceding step, N,N-diisopropylethylamine (0.6 mL, 4.7 mmol) and anhydrous dimethyl sulfoxide (0.3 mL, 4.2 mmol) in anhydrous dichloromethane (15 mL). The reaction mixture was stirred at ambient temperature for 1 hour and then quenched with 10% aqueous citric acid (50 mL). The mixture was extracted into dichloromethane (3×50 mL), and the dichloromethane solution was washed with 10% aqueous citric acid (40 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane) to give the title compound as a pale yellow oil (450 mg, 80%). 1H-NMR (300 MHz, CDCl3) δ 9.82 (s, 1H), 8.35 (d, J=8.7 Hz, 1H), 8.27 (d, J=7.1 Hz, 1H), 7.72 (t, J=8.6 Hz, 1H), 6.59 (s, 1H), 6.49 (s, 1H), 6.44 (s, 1H), 4.17 (t, J=6.0 Hz, 2H), 2.85 (t, J=6.0 Hz, 2H), 2.21 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891909 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-e23ed87e2c1c491f8885e79b1161f9aa |
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| Source note | uspto-grants-1999_04 |
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