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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901103Generated: October 26, 2026

1-Bromo-3-chloropropane → 5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/901103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
SolventMethyl Ethyl KetoneHCID 6569—
Product5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl esterHCID 4511235674%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl-5-hydroxyindole-2-carboxylate (15 g, 73 mmol, 1.0 eq.) and 1-bromo-3-chloropropane (8.8 mL, 88 mmol, 1.2 eq.) in 2-butanone (200 mL) was added potassium carbonate (12.1 g, 88 mmol, 1.2 eq.). The reaction mixture was stirred 160 h at 80° C. The reaction mixture was cooled down and partitioned between ethyl acetate and water. The aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with water and brine then dried over sodium sulfate, filtered and concentrated in vacuo. The crude mixture was purified by column chromatography on silica eluting with cyclohexane/ethyl acetate 9:1 to yield 15.3 mg (74%) of the title compound as a light yellow solid. MS (m/e): 282.7 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361682B2
Source datasetuspto-grants-2008_04
ORD IDord-891340eab47746c18ea2a6b9e9b1bd4d
Source noteuspto-grants-2008_04