HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196813Generated: October 30, 2026
Iodine → 2-(5-tert-butyl-2-iminothiazol-3(2H)-yl)ethanesulfonamide
https://huagongshe.com/reaction/2196813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Dimethylbutanal | HCID 76335 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 2-Aminoethanesulphonamide monohydrochloride | HCID 3021549 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(5-tert-butyl-2-iminothiazol-3(2H)-yl)ethanesulfonamide | HCID 66661025 | 12.2% |
Reaction Steps
A mixture of 3,3-dimethylbutanal (2.15 mL, 17.1 mmol), triethylamine (2.2 mL, 15.6 mmol), 2-aminoethanesulfonamide-hydrochloric acid (2.5 g, 15.6 mmol), and 4 g of 4 Å molecular sieves (8-12 mesh beads) in acetonitrile (40 mL) was stirred at ambient temperature for 20 h. This material was filtered through Celite with acetonitrile (additional 25 mL) then potassium thiocyanate (2.0 g, 20.7 mmol) was added and the mixture was warmed to 50° C. Iodine (3.95 g, 15.6 mmol) was added and the mixture was stirred at 50° C. for 16 h then was cooled to ambient temperature. The mixture was stirred with 50 mL of 20% aqueous sodium metabisulfite for 1 h then the layers were separated and the aqueous layer was extracted with CH2Cl2 (3×10 mL). The combined organics were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the crude title compound (0.5 g, 1.9 mmol, 12.2% yield) which was carried on without further purification. MS (DCI/NH3) m/z 264 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-2addea5ee9a641589c6e7d591b95560a |
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| Source note | uspto-grants-2012_12 |
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