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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072593Generated: October 26, 2026

Potassium Carbonate → racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1072593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
Reactant{1-Methyl-2-[7-(benzyloxy)-1h-indol-3-yl]ethyl}-carbamic acid tert-butyl esterHCID 11485811—
SolventMethyl Ethyl KetoneHCID 6569—
Productracemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl esterHCID 6951856570.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

The crude {1-methyl-2-[7-hydroxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester from above (29.2 g, 102 mmol theory) is dissolved in methyl ethyl ketone (300 mL) and bromoacetonitrile (20.4 mL, 306 mmol) and potassium carbonate (33.8 g, 250 mmol) is added. The mixture is heated at 80° C. for 2 hours. The solids are removed by filtration, the cake is washed with methyl ethyl ketone, and the combined filtrates are concentrated by rotary evaporation. The crude product is purified by flash chromatography (500 g silica gel, eluted with 8×500 mL dichloromethane, 4×500 mL 5% ethyl acetate/dichloromethane, 6×500 mL 10% ethyl acetate/dichloromethane). The fractions containing product are concentrated and hexane is added to the solution to precipitate out the product affording 23.7 g (70.2% yield) of racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911463B2
Source datasetuspto-grants-2005_06
ORD IDord-2f4f310b00424901a50b0647432141ec
Source noteuspto-grants-2005_06