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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041870Generated: November 2, 2026

Tetrahydrofuran → HCID 69673475, compound

https://huagongshe.com/reaction/2041870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-(3-Butynyl)phthalimideHCID 11171619—
Reactant4-broMo-2-phenylthiazoleHCID 11831528—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 69673475HCID 6967347555.6%

Reaction Steps

Under a nitrogen atmosphere, 15 ml of tetrahydrofuran, 1.50 g of the 2-phenyl-4-bromothiazole obtained in the above described stage, and 3.8 ml of triethylamine were added to 221 mg of dichlorobis(triphenylphosphine)palladium, 60 mg of copper iodide, and 1.24 g of N-(3-butynyl)phthalimide. The obtained mixture was stirred under reflux for 4 hours. After completion of the stirring, the reaction solution was cooled to a room temperature, and a solid was then filtrated. The filtrate was concentrated, and the residue was then purified by column chromatography (Wako Gel C-200; toluene:ethyl acetate=9:1), so as to obtain 1.24 g of a phthalimide compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586505B2
Source datasetuspto-grants-2013_11
ORD IDord-dc51c24b68d347fba5055ed5ad1f1a54
Source noteuspto-grants-2013_11