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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274774Generated: October 31, 2026

Benzenesulfonyl chloride → 5,6-difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/2274774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
Reactant5,6-difluoro-3-iodo-1H-indoleHCID 118060416—
SolventTetrahydrofuranHCID 8028—
Product5,6-difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 11806028372.4%

Reaction Steps

To a solution of 5,6-difluoro-3-iodo-1H-indole (Intermediate 27; 930 mg; 3.33 mmol) in THF (20 mL) at 0° C. was added NaH (266.4 mg; 60%; 6.66 mmol) under nitrogen. The reaction mixture was stirred at r.t. for 15 minutes before a solution of benzenesulfonyl chloride (763.4 mg; 4.32 mmol) in THF (2 mL) was added dropwise. The reaction was stirred at r.t. for 12 hours, quenched with an ice-water mixture (60 mL) and extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered, concentrated, and purified by a silica gel chromatography (petroleum ether/EtOAc=10/1-3/1) to afford 1.01 g (72%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-d1f273ecb1fa4caa8ad0d1150e364d70
Source noteuspto-grants-2015_09