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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513247Generated: October 29, 2026

5-Iodoisatin → 3-Hydroxy-5-iodo-3-phenyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/513247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-IodoisatinHCID 88695—
ReactantHCID 178489560HCID 178489560—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Hydroxy-5-iodo-3-phenyl-1,3-dihydro-indol-2-oneHCID 117599670—

Reaction Steps

A solution of 3M 2-methoxyphenylmagnesium bromide (0.92 mL, 2.747 mmol) in Et2O is added drop wise to a suspension of 5-iodoisatin (300 mg, 1.099 mmol) in THF whilst cooling in ice. The mixture is then stirred at room temperature for 1 hour. The reaction mixture is quenched by adding ammonium chloride solution and extracted several times with ethyl acetate. The combined organic phases are washed several times with water, dried over MgSO4 and concentrated under reduced pressure. The precipitate is filtered off with suction, washed with very small amounts of ethyl acetate and dried. This afforded the desired product as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102684B2
Source datasetuspto-grants-2015_08
ORD IDord-2bb7e4d831be4e1ea0c9ebc7b380580b
Source noteuspto-grants-2015_08