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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707694Generated: October 30, 2026

Methyl iodide → HCID 18962034, compound

https://huagongshe.com/reaction/1707694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-(4-fluorophenyl)-1H-indole-2-carboxylateHCID 5133930—
SolventDimethylacetamideHCID 31374—
ProductHCID 18962034HCID 18962034—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 8.0 g. (28 mmol.) of ethyl 3-(4'-fluorophenyl)indole-2-carboxylate in 30 ml. of dry dimethylacetamide stirred under nitrogen at -10° C., 1.6 g. (33 mmol.) of sodium hydride is added. The reaction mixture is stirred at -10° C. under nitrogen for 45 min., 4.8 g. (32 mmol.) of methyl iodide is added at -10° C., and the reaction mixture is allowed to warm to room temperature and stirred under nitrogen at room temperature for 2 hrs. The reaction mixture is poured into 400 ml. of ice/water, neutralized with 4 ml. of 2N. hydrochloric acid and extracted several times with diethyl ether. The diethyl ether extracts are combined, washed with water, washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated at reduced pressure. The residue is purified by column chromatography utilizing a silica gel column and chloroform as the eluant. The fractions containing the product are combined and evaporated at reduced pressure, and the residue is crystallized from n-hexane/petroleum ether to obtain the product (7.6 g. (91%)), m.p. 61°-62° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354772
Source datasetuspto-grants-1994_10
ORD IDord-3236ddce62764a7693386d3c9f074f6f
Source noteuspto-grants-1994_10