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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015436Generated: November 2, 2026

2-Phenylethanol → ethyl 2,3-dimethyl-1-(2-phenylethyl)-1H-indole-5-carboxylate

https://huagongshe.com/reaction/1015436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanolHCID 6054—
ReactantEthyl 2,3-dimethyl-1H-indole-5-carboxylateHCID 612460—
ReactantCyanomethylenetrimethylphospholanHCID 66670364—
SolventTolueneHCID 1140—
Productethyl 2,3-dimethyl-1-(2-phenylethyl)-1H-indole-5-carboxylateHCID 1543893—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 211 mg portion of ethyl 2,3-dimethyl-1H-indole-5-carboxylate was dissolved in 10 ml of toluene, and 0.232 ml of 2-phenylethanol and 224 mg of cyanomethylene trimethylphospholan were added at room temperature, followed by stirring at 100° C. for 17 hours. After evaporation of the solvent under a reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:49 to 1:9) to obtain 107 mg of ethyl 2,3-dimethyl-1-(2-phenylethyl)-1H-indole-5-carboxylate as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985764B2
Source datasetuspto-grants-2011_07
ORD IDord-5b1399b305974b06951770ab3ccf60b2
Source noteuspto-grants-2011_07