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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8330Generated: October 23, 2026

Benzenesulfonyl chloride → 4-Bromo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/en/reaction/8330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-BromoindoleHCID 676494—
Product4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—

Reaction Steps

4-Bromo-1-(benzenesulfonyl)-1H-indole was prepared from 4-bromoindole and phenylsulfonyl chloride according to Method 4 to afford 3.1 g (91%) of a light purple solid: 1HNMR (CDCl3) δ 7.94 (d, J=8 Hz, 1H), 7.89–7.84 (m, 2H), 7.62 (d, 4 Hz, 1H), 7.57–7.51 (m, 1H), 7.46–7.37 (m, 3H), 7.19–7.13 (m, 1H), 6.72 (dd, J=1, 4 Hz, 1H); MS (ESI) 419.9+421.9 (M+H)+; Purity (HPLC) >95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087750B2
Source datasetuspto-grants-2006_08
ORD IDord-dc1c665ddaab44ba8bee25485097fb45
Source noteuspto-grants-2006_08