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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264125Generated: October 26, 2026

Iodine → N-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamide

https://huagongshe.com/reaction/2264125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantN-(tert-butyl)-2-methoxybenzenesulfonamideHCID 23448664—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamideHCID 23151662—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 30.00 g (123.29 mmol) of N-(tert-butyl)-2-methoxybenzenesulfonamide in 400 ml of tetrahydrofuran is cooled to −70° C. and slowly admixed with a solution of 110.96 ml (277.41 mmol) of a 2.5 molar n-butyllithium solution in THF. The solution is subsequently warmed briefly to −30° C. and then cooled again to −60° C. At this temperature a solution of 31.29 g (123.29 mmol) of iodine in 200 ml of tetrahydrofuran is added dropwise. Subsequently the reaction solution is stirred at room temperature overnight. Following extraction with water, the organic phase is dried over sodium sulfate and evaporated to dryness. This gives 42.40 g (93% of theory) of N-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855166B2
Source datasetuspto-grants-2010_12
ORD IDord-3f93c616012f444e9f01790214c63b9c
Source noteuspto-grants-2010_12