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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349002Generated: October 27, 2026

Water → Ethyl 3-butyl-1-methyl-1H-indole-5-carboxylate

https://huagongshe.com/reaction/349002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactantethyl 3-butyl-1H-indole-5-carboxylateHCID 21086100—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 3-butyl-1-methyl-1H-indole-5-carboxylateHCID 2108610146.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of ethyl 3-butyl-1H-indole-5-carboxylate (0.6 g) in methylsulfoxide (10 mL) was added potassium t-butoxide (0.29 g) and iodomethane (2.0 mL). The mixture was stirred at 50° C. for 18H, at which time the mixture was pored into water (50 mL). The solution was extracted with ethyl acetate and the organic extracts washed three times with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Column chromatography on silica gel (100 mL) using 5% ethyl acetate in hexanes as eluent to give 0.294 g of the title compound: 1H NMR (CDCl3) δ 0.953, 1.44, 1.69, 2.77, 3.76, 4.40, 6.87, 7.26, 7.91, 8.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-aa76c3f36433495780bceeda6063faa4
Source noteuspto-grants-2007_02