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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073517Generated: November 2, 2026

Chlorosuccinimide → HCID 14154432, compound

https://huagongshe.com/reaction/1073517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-{[2-(4-Phenoxyphenoxy)ethyl]sulfanyl}pyrimidineHCID 13386760—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 14154432HCID 1415443274.7%

Reaction Steps

To a solution of 2-[2-(4-phenoxyphenoxy)ethylthio]pyrimidine (324 mg, 1.0 mmol) in carbon tetrachloride (3 ml), there was added N-chlorosuccinimide (160 mg, 1.2 mmol) with stirring under ice-cooling. The reaction system was gradually elevated to room temperature, and stirring was continued overnight. The precipitate was separated by filtration, and the filtrate was concentrated. Recrystallization of the residue from cyclohexane gave 2-[1-chloro-2-(4-phenoxyphenoxy)ethylthio]pyrimidine (268 mg) as pale yellow crystals. M.P., 86.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970222
Source datasetuspto-grants-1990_11
ORD IDord-bf4a00841ed4473086c8d20203e313e2
Source noteuspto-grants-1990_11