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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348968Generated: October 25, 2026

Butyl iodide → Methyl 1-butyl-4-iodo-1H-indole-6-carboxylate

https://huagongshe.com/reaction/348968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium HydroxideHCID 14797—
Reactantmethyl 4-iodo-1H-indole-6-carboxylateHCID 851585—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-butyl-4-iodo-1H-indole-6-carboxylateHCID 21086136—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of methyl 4-iodo-1H-indole-6-carboxylate (1.0 g) in DMF (10 mL) was added potassium hydroxide (0.392 g) and 1-iodobutane (0.8 mL). The mixture was heated to 80° C. for 18 h. The mixture was cooled to room temperature and partitioned between water and ethyl acetate. The layers were separated and the organic layer washed twice with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Column chromatography on silica gel (100 mL) using 20% ethyl acetate in hexanes as eluent to give 0.73 g of the title compound: 1H NMR (CDCl3) δ 0.940, 1.32, 1.81, 3.95, 4.15, 6.45, 7.31, 8.09, 8.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-b85ba07897364fb493119f93cc386d1a
Source noteuspto-grants-2007_02