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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264458Generated: October 28, 2026

Water → (R)-2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethylamine fumarate

https://huagongshe.com/reaction/264458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant(R)-N-[2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethyl]-trifluoroacetamideHCID 54398429—
SolventMethanolHCID 887—
Product(R)-2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethylamine fumarateHCID 6771397269%

Reaction Steps

A mixture of 0.97 g of (R)-N-[2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethyl]-trifluoroacetamide, 1 g of potassium hydroxide, 2 ml of water and 40 ml of methanol was boiled under reflux for 15 hours. The reaction mixture was subsequently poured into 80 ml of 1N sodium hydroxide solution, extracted twice with 80 ml of diethyl ether each time and once with 80 ml of ethyl acetate and the combined organic phases were washed once with 120 ml and dried over magnesium sulfate. After concentration in a vacuum, the residue was dissolved in 100 ml of anhydrous diethyl ether, filtered and treated while stirring with a solution of 322 mg of fumaric acid in 30 ml of methanol. The mixture was stirred at room temperature for 3 hours and the white crystals were subsequently filtered off. 600 mg (69%) of (R)-2-(8-methoxy-1H-benz[g]indol-1-yl)-1-methyl-ethylamine fumarate (1:0.5) with m.p. 209° were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-21ec4f99497f4fec85108b0a6ca34284
Source noteuspto-grants-1997_07