Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556699Generated: October 30, 2026

Iodine → tert-butyl 3-((5-tert-butyl-2-iminothiazol-3(2H)-yl)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/556699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium PyrosulfiteHCID 656671—
ReactantTert-butyl 3-(aminomethyl)azetidine-1-carboxylateHCID 10679125—
SolventAcetonitrileHCID 6342—
Producttert-butyl 3-((5-tert-butyl-2-iminothiazol-3(2H)-yl)methyl)azetidine-1-carboxylateHCID 6666069472%

Reaction Steps

A mixture of 3,3-dimethylbutanal (3.7 mL, 30 mmol), tert-butyl 3-(aminomethyl)azetidine-1-carboxylate (Astatech, 5 g, 27 mmol), and 8 g of 4 Å molecular sieves (8-12 mesh beads) in acetonitrile (50 mL) was stirred at ambient temperature for 72 h. The material was filtered through Celite with acetonitrile (additional 25 mL) then potassium thiocyanate (3.5 g, 35 mmol) was added and the mixture was warmed to 50° C. Iodine (6.8 g, 26.8 mmol) was added and the mixture stirred at 50° C. for 16 h then was cooled to ambient temperature. The mixture was stirred with 75 mL of 20% aqueous sodium metabisulfite for 1 h then the layers were separated and the aqueous layer was extracted with 3×10 mL CH2Cl2. The combined organics were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the crude title compound (6.3 g, 19 mmol, 72% yield) which was carried on without further purification. MS (DCI/NH3) m/z 326 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058293B2
Source datasetuspto-grants-2011_11
ORD IDord-b416ed3f2e32444aa508e0623c702353
Source noteuspto-grants-2011_11