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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254683Generated: October 30, 2026

Iodine → HCID 66851827, compound

https://huagongshe.com/reaction/254683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant18-Crown-6HCID 28557—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantNeopentylamineHCID 79882—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 66851827HCID 6685182759.8%

Reaction Steps

To a solution of 3,3-dimethylbutanal (Aldrich) (3.99 g, 39.8 mmol) in of acetonitrile (40 mL) was added 4 g of molecular sieves (4A beads, 8-12 mesh) and 2,2-dimethylpropan-1-amine (Aldrich) (3.16 g, 36.2 mmol). The mixture was stirred for 12 h at room temperature. The mixture was filtered and to the filtrate was successively added potassium thiocyanate (4.68 g, 48.1 mmol) and 1,4,7,10,13,16-hexaoxacyclooctadecane (1.24 g, 4.71 mmol). The temperature was adjusted at 50° C. and the mixture was stirred until all solids were dissolved then iodine (18.4 g, 72.4 mmol) was added. The reaction was stirred at 50° C. for 12 h. The reaction mixture was cooled to room temperature and diluted with EtOAc. The solution was washed with a solution of sodium metabisulfate. The aqueous layers was brought to pH=9 by adding NaOH (25%) and extracted with EtOAc. The Organic extracts were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was crystallized from EtOAc/Hexane to give 4.9 g of the title compound. MS (ESI+) m/z 227 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875640B2
Source datasetuspto-grants-2011_01
ORD IDord-3efc94d5f54d45ad9294e2bbd99c6019
Source noteuspto-grants-2011_01