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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340646Generated: October 26, 2026

Iodine → HCID 66851869, compound

https://huagongshe.com/reaction/340646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriethylamineHCID 8471—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantPotassium thiocyanateHCID 516872—
Reactant3,3,3-Trifluoropropylamine hydrochlorideHCID 25210505—
SolventAcetonitrileHCID 6342—
ProductHCID 66851869HCID 66851869—

Reaction Steps

A mixture of 3,3-dimethylbutanal (0.64 g, 6.0 mmol), 3,3,3-trifluoropropan-1-amine hydrochloride (Oakwood) (0.9 g, 6.0 mmol), 2 g of 4 Å (8-12 mesh beads) molecular sieves, and triethylamine (0.84 mL, 6.0 mmol) in 9 mL of dry acetonitrile was stirred for 20 hours at ambient temperature. The mixture was filtered through Celite and washed with 8 mL of acetonitrile. Potassium thiocyanate (0.78 g, 8.0 mmol) was added and the mixture warmed to 50° C. Iodine (1.5 g, 6.0 mmol) was added and the reaction stirred at 50° C. for 6 hours. To the mixture 10 mL of 20% Na2S2O5 was added, and stirring continued for 30 minutes. The organic layer was separated, dried with Na2SO4, filtered, and the solvent removed under reduced pressure. The resulting solid was used without further purification. 1H NMR (500 MHz, ACETONITRILE-D3) δ ppm 1.30 (s, 9H), 2.72-2.84 (m, 2H), 4.28 (t, J=6.87 Hz, 2H), 6.92 (s, 1H). MS (DCI/NH3) m/z 253.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895592B2
Source datasetuspto-grants-2014_11
ORD IDord-afb3e1927dbd464c9ce7da5b009f5209
Source noteuspto-grants-2014_11