Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811447Generated: November 1, 2026

Butyl iodide → HCID 86613947, compound

https://huagongshe.com/reaction/1811447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium bisulfateHCID 516920—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86613946HCID 86613946—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 86613947HCID 8661394741%

Reaction Steps

55.5 mg of potassium tert-butoxide was added to a DMSO solution (1 ml) of 90 mg of 5-(1-benzyl-8-hydroxy-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl)thiazolidine-2,4-dione, followed by stirring at room temperature for 1 hour. 29.8 μl of 4-iodobutane was added thereto, followed by stirring at room temperature for 2 hours. Water was added to the reaction liquid, potassium hydrogensulfate was added to the mixture, and the mixture was extracted with ethyl acetate. After washing with water, the extract was dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by preparative silica gel thin layer chromatography (dichloromethane:methanol=20:1), giving 42 mg (41% yield) of 5-(1-benzyl-8-butoxy-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl)thiazolidine-2,4-dione as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362252B2
Source datasetuspto-grants-2013_01
ORD IDord-808bf95ecf9343a9b55e4eaf131fb2cf
Source noteuspto-grants-2013_01