Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028180Generated: November 4, 2026

Iodine → HCID 68772367, compound

https://huagongshe.com/reaction/1028180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantButylamineHCID 8007—
ReactantPotassium thiocyanateHCID 516872—
Reactant3-OxotetrahydrofuranHCID 529392—
SolventAcetonitrileHCID 6342—
ProductHCID 68772367HCID 6877236720.2%

Reaction Steps

To a solution of dihydrofuran-3(2H)-one (0.5 g, 6.0 mmol, Small Molecules Inc.) in acetonitrile (10 mL) were added molecular sieves (0.5 g) and butan-1-amine (0.4 g, 5.5 mmol, Aldrich). The reaction mixture was stirred at room temperature overnight and then filtered. To the filtrate was added potassium thiocyanate (0.7 g, 7.3 mmol, Aldrich). The temperature was adjusted to 50° C. and the mixture was stirred until the solids were dissolved. Then, iodine (2.8 g, 10.9 mmol, EMD Chemicals) was added to the mixture and stirred at 50° C. overnight. The reaction mixture was cooled, concentrated and dissolved in EtOAc (15 mL). The solution was washed with Na-meta-bisulfite 20% (15 mL) by mixing the layers for 30 minutes. The organic layer was washed twice with 1N HCl (15 mL). The aqueous layers (metabisulfite and HCl) were combined and the pH was adjusted to pH ˜9 by adding NH4OH. The product was extracted with EtOAc (4×20 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to obtain the crude product (0.22 g) of the title compound. MS (ESI+) m/z 199 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735434B2
Source datasetuspto-grants-2014_05
ORD IDord-180b65222ca44fa8a28cb8a7916dee97
Source noteuspto-grants-2014_05