HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706883Generated: October 30, 2026
Water → 3-Chloro-4-(2-(2-methoxyethoxy)ethylthio)benzenesulfonamide
https://huagongshe.com/reaction/706883
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-4-fluorobenzenesulfonamide | HCID 7509883 | — |
| Reactant | 2-(2-Methoxyethoxy)ethane-1-thiol | HCID 11400802 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-4-(2-(2-methoxyethoxy)ethylthio)benzenesulfonamide | HCID 67126664 | — |
Reaction Steps
In a 25 mL microwave tube was added sodium hydride (0.6 g) in tetrahydrofuran (10 mL) to give a suspension. 2-(2-Methoxyethoxy)ethanethiol (1 g) was added slowly. After stirring for 30 minutes, 3-chloro-4-fluorobenzenesulfonamide (1.54 g) dissolved in 10 mL tetrahydrofuran was added slowly. The mixture was heated at 110° C. for 30 minutes in a Biotage Initiator microwave reactor. Water was added, the product was extracted with ether (20 mL×3), dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. The crude product was purified by flash chromatography on silica eluting with 0-25% ethyl acetate in hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174982B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-1123995efa294aa4ba04185bc9e0e5d7 |
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| Source note | uspto-grants-2015_11 |
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