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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76375Generated: October 25, 2026

Sodium hydride → 9-(Benzenesulfonyl)-1-bromocarbazole

https://huagongshe.com/reaction/76375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Iodobenzene-1-sulfonyl chlorideHCID 627400—
Reactant1-Bromo-9H-carbazoleHCID 11230335—
SolventTetrahydrofuranHCID 8028—
Product9-(Benzenesulfonyl)-1-bromocarbazoleHCID 67405182—

Reaction Conditions

Temperature40 °C

Reaction Steps

19.6 g (80 mmol) of 1-bromocarbazole are initially introduced in 1000 ml of THF, and 8.9 g (223.3 mmol) of NaH (60% in oil) are added at 0° C. 24 g (80 mmol) of 2-iodobenzenesulfonyl chloride are subsequently added to the mixture, which is then stirred at 40° C. for 12 h. The organic phase is dried over MgSO4, and the solvent is removed in vacuo. The residue is recrystallised from acetone and finally sublimed in a high vacuum. Yield: 29 g (574 mmol), 72% of theory, purity according to HPLC 99.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835626B2
Source datasetuspto-grants-2014_09
ORD IDord-3c43d7a676ae43afb3bbd4062c96f588
Source noteuspto-grants-2014_09