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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14221Generated: October 25, 2026

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

https://huagongshe.com/reaction/14221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantMethyl indole-6-carboxylateHCID 639844—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Productmethyl 1-butyl-1H-indole-6-carboxylateHCID 21086134—

Reaction Steps

Methyl 1H-indole-6-carboxylate (4.17 g) was dissolved in DMSO (30 mL), and potassium tert-butoxide (2.93 g) was added. The mixture was stirred for ten min at room temperature. Iodobutane (3.0 mL) was added. The mixture was allowed to stir for three additional hours. The mixture was partitioned between ethyl acetate and water and brine, dried over sodium sulfate, filtered, and concentrated to give methyl 1-butyl-1H-indole-6-carboxylate (4.53 g). MS (ESI+) for C14H17NO2+H1 m/z 232.12 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-986f12927c2143d6a3c663c2a48c33dd
Source noteuspto-grants-2010_06