Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710521Generated: October 31, 2026

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

https://huagongshe.com/reaction/1710521

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 numberUS07790716B2
Source datasetuspto-grants-2010_09
ORD IDord-266a93fff7c3404787c1679309bc4446
Source noteuspto-grants-2010_09