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HRID 538817Erstellt: 26. Oktober 2026

Iodine → 3-isobutyl-4,4,6,6-tetramethyl-4,6-dihydrofuro[3,4-d]thiazol-2(3H)-imine

https://huagongshe.com/reaction/538817

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktIsobutylamineHCID 6558—
Edukt2,2,5,5-Tetramethyltetrahydro-3-ketofuranHCID 138511—
EduktPotassium thiocyanateHCID 516872—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-isobutyl-4,4,6,6-tetramethyl-4,6-dihydrofuro[3,4-d]thiazol-2(3H)-imineHCID 6685185923%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 2,2,5,5-tetramethyldihydrofuran-3(2H)-one (2.0 g, 14.1 mmol, Aldrich) in acetonitrile (10 mL) were added molecular sieves (2.0 g) and 2-methylpropan-1-amine (1.0 mL, 12.8 mmol, Aldrich). The reaction mixture was stirred at 60° C. for 48 hr and then filtered through celite. To the filtrate were added potassium thiocyanate (1.65 g, 17.0 mmol, Aldrich). The reaction mixture was stirred at 60° C. until the solids were dissolved and then iodine (6.5 g, 25.6 mmol, EMD chemicals) was added. The reaction mixture was stirred 60° C. for 48 hr, cooled, concentrated and dissolved in ethyl acetate (15 mL). The solution was washed with sodium metabisulfite 20% (35 mL) by mixing the layers for 30 min. The organic layer was washed twice with HCl 1N (35 mL). The aqueous layers (sodium metabisulfite and HCl) were combined and the pH was adjusted to pH˜9 by adding NH4OH and then extracted with ethyl acetate (4×40 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to obtain the crude product (0.75 g) of the title compound. MS (ESI+) m/z 255 (M+H)+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865753B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-299d157b86244b92b580a239500833ff
Quellennotizuspto-grants-2014_10