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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215671Generated: October 31, 2026

Sodium Iodide → HCID 21952553, compound

https://huagongshe.com/reaction/2215671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 21952555HCID 21952555—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 21952553HCID 21952553—

Reaction Steps

To a mixture of trimethylsilyl chloride (0.19 mL, 1.5 mmol), sodium iodide (224 mg, 1.5 mmol) and acetonitrile (61 mg, 1.5 mmol) was added dropwise a solution of 5-ethyl-8-isopropyl-11-hydroxy-11-phenyl-5,10-dihydro-11H-indeno[1,2-b]quinolin-10-one in 1,2-dichloroethane with stirring at room temperature. The mixture was stirred at 50° C. overnight followed by allowing to cool to room temperature. The reaction mixture was treated diluted aqueous solution of sodium sulfite. The separated organic layer was washed with water four times and then with saturated sodium chloride solution followed by drying with sodium sulfate. After removing the solvent, the residue was purified by silica gel-chromatography (chloroform) followed by crystallization from diethyl ether to give the title compound. 1H-NMR (CDCl3) δ 1.30 (6H, d, CH(CH3)2), 1.79 (3H, t, NCH2CH3), 3.05 (1H, septet, CH), 4.81 (2H, q, NCH2), 5.18 (1H, s, H-11), 7.16-7.64 (10H, m, Ar—H), 7.96 (1H, d, H-6), 8.37 (1H, d, H-9)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109338B2
Source datasetuspto-grants-2006_09
ORD IDord-2767cc90834d4b6dab3794f60ec78415
Source noteuspto-grants-2006_09