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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217088Generated: October 31, 2026

Acetic Acid → 3-Methyl-N-propyl-1H-indol-1-amine

https://huagongshe.com/reaction/2217088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Methyl-N-propylidene-1H-indol-1-amineHCID 68863078—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Methyl-N-propyl-1H-indol-1-amineHCID 2194606396%

Reaction Conditions

Temperature30 °C

Reaction Steps

In a 800 L vessel, prepare a solution of 3.0 kg (74.4 mol) sodium borohydride and 26.8 kg (124 mol, 86% purity) 3-methyl-N-(propylidene)-1H-indol-1-amine in 108 kg NMP. Prepare a solution of 4.5 kg (74.4 mol) glacial acetic acid in 27 kg NMP. Add the acetic acid solution over a period of about 30 nm at 30° C. to the sodium borohydride solution. Immediately hydrogen is evolved. Stir the reaction mixture at 30° C. until completion of the reaction (˜1 h). Add 6.3 kg ethanol to the reaction mixture, foaming occurs immediately. The reaction mixture is then worked-up by adding additional 80 L water cautiously. Attention is taken during the addition of water such that foaming is controlled, slow addition of water is recommended especially in the beginning to avoid uncontrolled foaming. Care is taken to ensure no or only minimal foaming occurs while the first 1–2 L of water is added. The reaction mixture is allowed to stand over night. Extract the water phase three times with 45 kg n-heptane and wash the combined organic phases with 66 L water. Evaporate the combined organic phases to dryness. This results in 22.4 kg 3-methyl-N-propyl-1H-indol-1-amine (yield 90%, 94% purity) as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112682B2
Source datasetuspto-grants-2006_09
ORD IDord-cfa297d152bc4aef9f8cb3d3b4cedcd4
Source noteuspto-grants-2006_09