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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400588Generated: October 25, 2026

Tetrabutylammonium Fluoride → N-(4-Bromo-2-iodophenyl)benzenesulfonamide

https://huagongshe.com/reaction/400588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantN,N-bisbenzenesulfonyl-(4-bromo-2-iodoaniline)HCID 60026850—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-(4-Bromo-2-iodophenyl)benzenesulfonamideHCID 6002630790.2%

Reaction Steps

A solution of tetrabutylammonium fluoride (1 M in THF, 11 mL) in 30 mL of THF was treated with N,N-bisbenzenesulfonyl-(4-bromo-2-iodoaniline) (5.78 g, 10 mmol) in several portions. After 18 hours, the mixture was diluted with of 40 mL of ethyl acetate and 40 mL of 1 N HCl. The phases were separated and the aqueous layer was extracted with two 40 mL portions of ethyl acetate. The combined organic layers were washed with two 20 mL portions of 1 N HCl, two 20 mL portions of saturated aqueous sodium bicarbonate solution, 20 mL of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 3.95 g (90% yield) of the title compound as a solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-f48f7c3ff64b4f578e03f54458b9a514
Source noteuspto-grants-2014_06