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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413033Generated: October 31, 2026

Acetic Acid → N,N-Dimethyl-1-(2-methyl-1H-indol-3-yl)methanamine

https://huagongshe.com/reaction/2413033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
Reactant2-MethylindoleHCID 7224—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductN,N-Dimethyl-1-(2-methyl-1H-indol-3-yl)methanamineHCID 181513—

Reaction Steps

AcOH, 236 ml., was mixed with cooling and stirring with 62 ml. of 37% formaldehyde at 10°, and 154 ml of 25% aqueous dimethylamine was added dropwise with cooling so as to maintain the temperature at 10°. A solution of 100 g of 2-methylindole in 160 ml of dioxane was then added dropwise with cooling, again maintaining the temperature at 10°. The mixture was stirred at ice temperature for 1 hour and then overnight at room temperature. The mixture was then poured into 2.0 of water with stirring. A small amount of insoluble material was removed by filtration. The filtrate was treated with activated charcoal, filtered again, and the filtrate cooled and basified by the dropwise addition of about 225 ml. of 50% aqueous sodium hydroxide. The product was collected by filtration, washed with water, and air dried, yield 96 g. This material was dissoved in 700 ml of dilute aqueous HCl, treated with activated carbon, filtered, and again basified after diluting to 2 1. with water.The product was collected, air dried, and recrystallized from acetonitrile, yield 72 g., m.p. 117°-119°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495352
Source datasetuspto-grants-1985_01
ORD IDord-2426a1dfdcae43bfa71b57313ba4154d
Source noteuspto-grants-1985_01