Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843940Generated: October 30, 2026

Sodium Iodide → HCID 54471240, compound

https://huagongshe.com/reaction/843940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
Reactant6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazoleHCID 22611308—
SolventAcetonitrileHCID 6342—
ProductHCID 54471240HCID 5447124079.1%

Reaction Steps

To a solution of 0.32 gm (1.1 mMol) 6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole in 8 mL acetonitrile were added 0.30 gm (1.68 mMol) potassium carbonate, 0.25 gm (1.68 mMol) sodium iodide and 0.23 mL (1.68 mMol) 2-phenyl-1-ethyl bromide. The resulting mixture was stirred 4 hours at room temperature followed by 5 hours at reflux. The reaction mixture was cooled to room temperature and then partitioned between dichloromethane and water. The aqueous phase was extracted well with dichloromethane. All of the organic phases were combined, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 7% methanol in dichloromethane. Fractions shown to contain product were concentrated under reduced pressure to give 0.345 gm (79%) of the desired compound. A portion was converted to the corresponding hydrochloride salt,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380201B1
Source datasetuspto-grants-2002_04
ORD IDord-6db44d7777d74697b78f96454f9b2ac3
Source noteuspto-grants-2002_04