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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811448Generated: November 1, 2026

Benzyl Bromide → HCID 86646468, compound

https://huagongshe.com/reaction/1811448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium bisulfateHCID 516920—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86613946HCID 86613946—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 86646468HCID 8664646876%

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. 30 μl of benzyl bromide was added thereto, followed by stirring at room temperature for 1 hour. Water was added to the reaction liquid, potassium hydrogensulfate was added to the mixture, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by preparative silica gel thin layer chromatography (dichloromethane:methanol=20:1), giving 84.5 mg (76% yield) of 5-(1-benzyl-8-benzyloxy-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-e5a07db3e369435a91d7fed6208d67e3
Source noteuspto-grants-2013_01