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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362044Generated: October 30, 2026

Water → 1-(1H-indol-5-yl)-N-methylmethanamine

https://huagongshe.com/reaction/1362044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantIndole-5-carboxaldehydeHCID 589040—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(1H-indol-5-yl)-N-methylmethanamineHCID 1722179491%

Reaction Steps

Indole-5-carbaldehyde (1.0 g, 6.9 mmol) was dissolved in anhydrous methanol (15 mL). Methylamine (9.9 mL of 2M solution in methanol, 19.8 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 (20 mL). Sodium borohydride (262 mg, 6.9 mmol) was added and the mixture was stirred overnight. Water (1 mL) was added and the solution was concentrated. 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 a brown oil (980 mg, 91%). 1H NMR (200 MHz, CDCl3) δ 8.60 (s, 1H), 7.56 (s, 1H), 7.35-7.15 (m, 3H), 6.55 (m, 1H), 3.85 (s, 2H), 2.49 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-263f631050de41808201f5000c32fc48
Source noteuspto-grants-2011_02