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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475306Generated: October 31, 2026

Chlorosulfonic acid → 1-acetyl-5-bromo-2,3-dihydro-1H-indole-6-sulfonyl chloride

https://huagongshe.com/reaction/1475306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant1-(5-bromo-2,3-dihydro-1H-indol-1-yl)ethan-1-oneHCID 721847—
Product1-acetyl-5-bromo-2,3-dihydro-1H-indole-6-sulfonyl chlorideHCID 14024584—

Reaction Steps

1-(5-Bromo-2,3-dihydro-indol-1-yl)-ethanone (0.249 g, 1.04 mmol) was added portionwise to chlorosulfonic acid (1 mL) at 20° C. with stirring and mixture was stirred for 26 h, then poured onto crushed ice. The resulting solid was collected by filtration and dried in vacuo. The filtrate was extracted with EtOAc and the organic phase was dried (Na2SO4) and evaporated in vacuo to give further solid. The two batches of solid were combined to give the title compound (0.25 g) which was used in the next stage without further purification. MS: [M−H]−=336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018214B2
Source datasetuspto-grants-2015_04
ORD IDord-1e72ac46393a4772a7eb38f8389cb7ab
Source noteuspto-grants-2015_04