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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510871Generated: October 30, 2026

N-Iodosuccinimide → 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone

https://huagongshe.com/reaction/510871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5'-Chloro-2'-hydroxy-4'-methylacetophenoneHCID 598229—
SolventAcetic AcidHCID 176—
Product1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanoneHCID 11472394—

Reaction Steps

To a stirred solution of 1-(5-chloro-2-hydroxy-4-methylphenyl)ethanone (20 g, 110 mmol) in acetic acid (200 mL) was added N-iodosuccinimide (29 g, 130 mmol) and the resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo, neutralized with saturated sodium bicarbonate, filtered off insoluble succinimide and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude product was recrystallized from a mixture of ethyl acetate and hexane (25.8 mg, 77%). LCMS calculated for C9H9ClIO2 (M+H)+: m/z=311.0. found: 311.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-9ca9c602a3cc4166a7dfb78be86487eb
Source noteuspto-grants-2015_08