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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14225Generated: October 26, 2026

Butyl iodide → butyl 1-butyl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/14225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
Reactant1-butyl-1H-indole-6-carboxylic acidHCID 21085167—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Productbutyl 1-butyl-1H-indole-6-carboxylateHCID 21086016—

Reaction Steps

1-Butyl-1H-indole-6-carboxylic acid (0.450 g) was dissolved in dimethyl sulfoxide (10 mL). Potassium tert-butoxide (0.317 g) was added and the mixture was stirred for 10 min at room temperature. Iodobutane (0.33 mL) was added and the mixture was allowed to stir at room temperature for 6 h. Water was then added and the mixture was partioned between ethyl acetate, water, and brine, and dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography using heptane/dichloromethane (30/70) gave butyl 1-butyl-1H-indole-6-carboxylate (0.429 g). MS (ESI+) for C17H23NO2+H1 m/z 274.20 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-32acb31f6e0644ba9d336afcf69903fe
Source noteuspto-grants-2010_06