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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112655Generated: November 3, 2026

Iodoethane → 2-[N-(Benzyloxycarbonyl)-N-methylaminomethyl]-1-ethyl-1H-indole

https://huagongshe.com/reaction/2112655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant2-[N-(Benzyloxycarbonyl)-N-methylaminomethyl]-1H-indoleHCID 57440843—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[N-(Benzyloxycarbonyl)-N-methylaminomethyl]-1-ethyl-1H-indoleHCID 2259376587%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (60% dispersion in mineral oil, 0.25 g, 7.1 mmole) was added portionwise, allowing for gas evolution, to a solution of 2-[N-(benzyloxycarbonyl)-N-methylaminomethyl]-1H-indole (1.40 g, 4.75 mmole) in DMF (35 mL) at 0° C. When the NaH addition was complete, ethyl iodide (0.42 mL, 5.2 mmole) was added at 0° C. The reaction was stirred at 0° C. for 15 minutes then at RT overnight. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were dried over K2CO3 and concentrated to afford the title compound (1.30 g, 87%) as an orange solid: MS (ES) m/e 323 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524843B2
Source datasetuspto-grants-2009_04
ORD IDord-cb46d363ee3a47cfa152561da2b92410
Source noteuspto-grants-2009_04