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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387060Generated: October 27, 2026

4-Iodobenzoic acid → 4-Iodophenyl 2-[4-[2-(1-Pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl Ketone

https://huagongshe.com/reaction/1387060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodobenzoic acidHCID 12085—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[4-[2-(1-Pyrrolidinyl)ethoxy)phenyl]benzo[b]thiopheneHCID 10663708—
CatalystDimethylformamideHCID 6228—
CatalystTitanium TetrachlorideHCID 24193—
Solvent1,2-DichloroethaneHCID 11—
Product4-Iodophenyl 2-[4-[2-(1-Pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl KetoneHCID 21182628—

Reaction Conditions

Temperature0 °C

Reaction Steps

A slurry of 4-iodobenzoic acid (7.67 g, 30.9 mmol) in 300 mL of 1,2-dichloroethane and 2 drops of DMF was treated with SOCl2 (11.3 mL, 154.6 mmol). The resulting mixture was heated at reflux overnight. The clear solution was evaporated in vacuo, then the solid residue was resuspended in 1,2-dichloroethane and reconcentrated. The crude acid chloride was dissolved in 300 mL of 1,2-dichloroethane, and 2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophene (5.0 g, 15.5 mmol) was added. The solution was cooled to 0° C. and treated with TiCl4 (8.5 mL, 77.3 mmol). After 5.5 h, the reaction mixture was carefully poured into 600 mL of saturated aqueous NaHCO3. The layers were separated, and the aqueous phase was extracted with CHCl3 (3×300 mL). The combined organic phases were dried over Na2SO4, filtered, and concentrated in vacuo. Purification by PrepLC (SiO2; 1% MeOH in CHCl3, saturated with NH4OH) afforded 6.79 g (12.3 mmol; 79%) of the title product as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-351839297cd5403185c06292856f3e72
Source noteuspto-grants-2001_07