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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29402Generated: October 26, 2026

N-Iodosuccinimide → 5-Iodo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/29402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-Hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl esterHCID 13849456—
SolventCarbon TetrachlorideHCID 5943—
Product5-Iodo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871604038%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 4.4 g (17.7 mmol) of 4-hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester was added 40 mL of carbon tetrachloride, the mixture was cooled with an water/ice bath while 1 equivalent of N-iodosuccinimide was added in small portions. After stirring at 0° C. for 3 h, the reaction mixture was loaded onto a column and purified by column chromatography to give 2.55 g mg (38% yield) of 5-iodo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-187f88142621442abc544885715c3529
Source noteuspto-grants-2008_09