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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14157Generated: October 26, 2026

Butyl iodide → Methyl 1-butyl-1H-indole-5-carboxylate

https://huagongshe.com/reaction/14157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
Reactantmethyl 1H-indole-5-carboxylateHCID 2737635—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 1-butyl-1H-indole-5-carboxylateHCID 21086133—

Reaction Steps

To a mixture of methyl 1H-indole-5-carboxylate (6.0 g) in methylsulfoxide (30 mL) was added potassium t-butoxide (3.88 g). The mixture was stirred at room temperature for 10 minutes at which time 1-iodobutane (1.8 mL) was added. The mixture was stirred at room temperature for 5 h then partitioned between water and methylene chloride. The layers were separated and the organic layer washed three times with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Column chromatography on silica gel (100 mL) using 10% ethyl acetate in hexanes as eluent to give 6.18 g of the title compound: 1H NM (CDCl3) δ 0.923, 1.38, 1.83, 3.9, 4.14, 6.58, 7.15, 7.34, 7.9, 8.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-a47c178ea2044a14a353ff7a1b5f3343
Source noteuspto-grants-2010_06