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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226169Generated: November 1, 2026

N-Iodosuccinimide → HCID 15230229, compound

https://huagongshe.com/reaction/2226169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 18966551HCID 18966551—
CatalystSilver NitrateHCID 24470—
SolventAcetoneHCID 180—
ProductHCID 15230229HCID 1523022985.3%

Reaction Steps

To a stirred solution of 1-benzyl-3-propargyl-5,5-dimethylhydantoin (1.2 g, 4.6 mmole) in acetone (50 mL) at room temperature was added finely ground silver nitrate (0.15 g. 0.8 mmole), followed by N-iodosuccinimide (1.16 g, 5.2 mmole). The reaction mixture was stirred at room temperature for 5 hr. The reaction mixture was then passed through Celite by suction filtration and washed with acetone. The titrate was concentrated on a rotary evaporator and diluted with ethyl acetate. The solution was washed with water and brine and dried over sodium sulfate. The solvent was evaporated on a rotary evaporator to give 1.5 g of 1-benzyl-3-(3-iodo-2-propynyl)-5,5-dimethylhydantoin as a solid, mp=109°-112° C. An NMR spectrum also showed the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346913
Source datasetuspto-grants-1994_09
ORD IDord-c0fd6277614a497789f1e75a5f6d95e1
Source noteuspto-grants-1994_09