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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430394Generated: November 2, 2026

N-Iodosuccinimide → HCID 58017974, compound

https://huagongshe.com/reaction/1430394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 68802901HCID 68802901—
SolventAcetonitrileHCID 6342—
ProductHCID 58017974HCID 5801797487.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

5.30 g (26.0 mmol) of 2-chloro-4-hexylthiazole and 7.02 g (31.2 mmol) of N-iodosuccinimide were dissolved in 40 mL of acetonitrile, and stirred for 2 hours at 50° C. under argon gas purge. The resultant reaction mixed liquid was washed with a Na2S203 aqueous solution, and the aqueous layer was extracted with chloroform and added to the organic layer. The organic layer was concentrated, and subjected to silica gel column chromatography (development solvent:chloroform/hexane=1/1 (volumetric ratio)) to take out red transparent liquid. Since a peak of a molecular weight of 330 containing one chlorine atom was observed in the mass spectrum (apparatus: HP-6890GC/HP-5973MSD, column: SGE BPX-5 (30 m×0.25 mm I.D.×025 μm), column temperature: 50° C. (5 minutes)→10° C./min.→350° C. (held for 5 minutes), injection port temperature: 280° C., carrier gas: He, 1.0 ml/min.), it could be confirmed that the above-described red transparent liquid was the intended 2-chloro-4-hexyl-5-iodothiazole. The amount obtained was 7.50 g, and the yield was 87.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940856B2
Source datasetuspto-grants-2015_01
ORD IDord-8d31e06b5e6f4daeb85de1577a43c333
Source noteuspto-grants-2015_01