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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium PyrosulfiteHCID 656671—
Reactant2-Aminoethanesulphonamide monohydrochlorideHCID 3021549—
SolventAcetonitrileHCID 6342—
Product2-(5-tert-butyl-2-iminothiazol-3(2H)-yl)ethanesulfonamideHCID 6666102512.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338467B2
Source datasetuspto-grants-2012_12
ORD IDord-2addea5ee9a641589c6e7d591b95560a
Source noteuspto-grants-2012_12