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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199710Generated: October 29, 2026

2-Bromoaniline → ethyl 7-bromo-3-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2199710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanilineHCID 11992—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Productethyl 7-bromo-3-(3-ethoxy-3-oxopropyl)-1H-indole-2-carboxylateHCID 68940416—

Reaction Conditions

Temperature19 °C

Reaction Steps

A mixture of 2-bromoaniline (34.2 g) in 5M HCl (50 mL) and water (250 mL) at 0° C. was treated with NaNO2 (13.8 g) in water (200 mL). After addition, sodium acetate (92.3 g) in water (250 mL) and 2-oxo-cyclopentanecarboxylic acid ethyl ester (30 mL) were added. The mixture was stirred for 15 minutes, warmed to 19° C. over two hours and extracted with dichloromethane. The extract was dried (MgSO4), filtered and concentrated. The concentrate was dissolved in 1.1:1 H2SO4:ethanol (30 mL), refluxed overnight, cooled to room temperature, quenched with water (1.5 L), and filtered. The filtrant was dissolved in dichloromethane (200 mL) and filtered through a Flash 75 cartridge with dichloromethane. After concentration, the product was recrystallized from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359296B2
Source datasetuspto-grants-2016_06
ORD IDord-6502f330eecf471d84a49b8233d2caad
Source noteuspto-grants-2016_06