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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711829Generated: October 25, 2026

Water → (1H-indol-7-ylmethyl)(methyl)amine

https://huagongshe.com/reaction/1711829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantIndole-7-carboxaldehydeHCID 2734629—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(1H-indol-7-ylmethyl)(methyl)amineHCID 5934034192%

Reaction Steps

Indole-7-carbaldehyde (500 mg, 3.4 mmol) was dissolved in anhydrous methanol (10 mL). Methylamine (5.1 mL of 2M solution in methanol, 9.55 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 (10 mL). Sodium borohydride (131 mg, 3.45 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 indole was extracted with ethyl acetate (3×20 mL), dried over MgSO4 and concentrated to afford the title compound as a yellow oil (484 mg, 92%). 1H NMR (300 MHz, CDCl3) δ 7.54 (s, 1H), 7.29-7.17 (m, 2H), 7.04 (d, J=3.1 Hz, 1H), 6.44 (d, J=3.1 Hz, 1H), 3.84 (s, 2H), 2.46 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-c52f905c27284a47a9c8ade62a7d78f5
Source noteuspto-grants-2010_09