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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993307Generated: November 1, 2026

Hydrochloric Acid → 5-Acetamido-6-benzoylindane

https://huagongshe.com/reaction/1993307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chlorideHCID 7412—
ReactantN-(2,3-Dihydro-1H-inden-5-yl)acetamideHCID 583823—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Acetamido-6-benzoylindaneHCID 2350561413%

Reaction Steps

To a solution of 5-acetamidoindane (1.0 g, 5.7 mmol) and benzoyl chloride (732 mL, 6.3 mmol) in 15 mL of CH2Cl2 at 0° C. was added AlCl3 (1.52 g, 11.4 mmol) as a solid. The mixture was stirred to rt overnight. A spatula full of AlCl3 was added and the mixture heated to reflux for 3 days. The solution was then poured into a mixture of concentrated HCl and ice, and stirred. The mixture was then diluted with water and extracted with 2×50 mL of CH2Cl2. The extract was washed with brine, then dried over MgSO4 and concentrated in vacuo. The crude residue was subjected to flash column chromatography eluting with EtOAc/hexane to give the title compound (200 mg, 13%). 1H NMR (CDCl3): 10.95 (s, 1H), 8.50 (s, 1H), 7.68 (d, 2H), 7.59 (t, 1H), 7.49 (t, 2H), 7.37 (s, 1H), 2.99 (t, 2H), 2.83 (t, 2H), 2.22 (s, 3H), 2.10 (p, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652006B2
Source datasetuspto-grants-2010_01
ORD IDord-da69282c16be4f4aadd87cf32303efc1
Source noteuspto-grants-2010_01