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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273841Generated: October 30, 2026

1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)propan-1-one → HCID 20094393, compound

https://huagongshe.com/reaction/273841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)propan-1-oneHCID 23003971—
CatalystSulfuric AcidHCID 1118—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20094393HCID 2009439379.1%

Reaction Steps

To a solution of 1-acetyl-5-propionylindoline (1.65 g) in tetrahydrofuran (150 ml) were added concentrated sulfuric acid (5 drops) and pyrrolidone hydrotribromide (4.14 g), and the mixture was stirred at room temperature for 16 hours. The insoluble materials were filtered off, and the filtrate was concentrated under reduced pressure. The residue was extracted with ethyl acetate, and the extract was washed with water, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was recrystallized from ethanol to give 1.78 g of 1-acetyl-5-(2-bromopropionyl)indoline melting at 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-f18b0b7521a6488896d1ec2f879e7208
Source noteuspto-grants-1995_02