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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711828Generated: October 26, 2026

Water → n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine

https://huagongshe.com/reaction/1711828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant1-methyl-1H-indole-5-carbaldehydeHCID 7537534—
SolventMethanolHCID 887—
Productn-Methyl-1-(1-methyl-1h-indol-5-yl)methanamineHCID 18525753100%

Reaction Steps

N-Methylindole-5-carbaldehyde (800 mg, 5.1 mmol) was dissolved in anhydrous methanol (15 mL). Methylamine (7.15 mL of 2M solution in methanol, 15.3 mmol) was added and the reaction was stirred for 3 hr. The solution was concentrated to a yellow oil and then dissolved into anhydrous methanol (15 mL). Sodium borohydride (194 mg, 5.1 mmol) was added and the mixture was stirred overnight. Water (1 mL) was added and the solution was concentrated to an orange oil. Sodium hydroxide (5 mL, 1N) was added and the product was extracted with ethyl acetate (3×20 mL), dried over MgSO4 and concentrated to afford the title compound as an orange oil (885 mg, 100%). 1H NMR (200 MHz, CDCl3) δ 7.57(s, 1H), 7.35-7.11(m, 3H), 6.51 (d, J=2.9 Hz, 1H), 3.85 (s, 2H), 3.79 (s, 3H), 2.48 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-21504158dc084497ad3ae3acd4fdeae6
Source noteuspto-grants-2010_09