Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749294Generated: October 25, 2026

Methyl iodide → Ethyl 4-benzyloxy-1-methylindole-2-carboxylate

https://huagongshe.com/reaction/749294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-(phenylmethoxy)-1H-indole-2-carboxylateHCID 119707—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-benzyloxy-1-methylindole-2-carboxylateHCID 22054863—

Reaction Steps

To a stirred suspension of sodium hydride (0.27 g, 60% dispersion in mineral oil) in DMF (50 mL) under nitrogen at room temperature was added ethyl 4-benzyloxyindole-2-carboxylate (1.59 gm). Methyl iodide (0.5 mL) was added 10 min. later. After 2 hr. excess sodium hydride was quenched with acetic acid (0.4 mL) and the solvent evaporated under reduced pressure. The residue was taken into EtOAc, washed with water and brine, dried over MgSO4, and evaporated to dryness to give an oil which was triturated with hexane to precipitate 1.45 g of the title compound. Mp 89-90.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402604B2
Source datasetuspto-grants-2008_07
ORD IDord-1aa8a9db03b541abab1cb95525cf4d22
Source noteuspto-grants-2008_07