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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847469Generated: October 30, 2026

Acetic Anhydride → 1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanone

https://huagongshe.com/reaction/1847469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(benzenesulfonyl)-2,3-dihydroindoleHCID 668757—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanoneHCID 14112956—

Reaction Steps

To a suspension of AlCl3 (144 g, 1.08 mol) in CH2Cl2 (1070 mL) was added acetic anhydride (54 mL). The mixture was stirred for 15 minutes before a solution of 1-(phenylsulfonyl)indoline (46.9 g, 0.180 mol) in CH2Cl2 (1070 mL) was added dropwise. The mixture was stirred for 5 h and was quenched by the slow addition of crushed ice. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organics were washed with saturated aqueous NaHCO3 and brine, dried over Na2SO4, and concentrated under vacuum to obtain 1-(1-(phenylsulfonyl)indolin-5-yl)ethanone (42.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952050B2
Source datasetuspto-grants-2015_02
ORD IDord-85e3f72d67614473ad4ddbbf2a1329aa
Source noteuspto-grants-2015_02