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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170603Generated: October 31, 2026

Methyl iodide → methyl 1H-indole-5-carboxylate

https://huagongshe.com/reaction/2170603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventAcetonitrileHCID 6342—
Productmethyl 1H-indole-5-carboxylateHCID 2737635—

Reaction Steps

To a solution of 1H-indole-5-carboxylic acid (1 g, 6.2 mmol, 1.0 equiv) in acetonitrile (40 mL) were added 1,8-Diazabicyclo[5.4.0]undec-7-ene (1.1 mL, 7.4 mmol, 1.2 equiv) and iodomethane (2.3 mL, 37.2 mmol, 6 equiv). The solution was stirred under reflux overnight. The reaction mixture was concentrated in vacuo. The residue was dissolved in AcOEt, washed with a 0.5 N HCl aqueous solution, a saturated NaHCO3 solution and brine, dried over MgSO4 and concentrated in vacuo. The obtained oil was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051265B2
Source datasetuspto-grants-2015_06
ORD IDord-49572d010f2544ff8f10f493c0c3d535
Source noteuspto-grants-2015_06