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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761091Generated: October 31, 2026

Acetic Acid → (1,3-dimethyl-1H-indol-2-yl)-N-methylmethanamine

https://huagongshe.com/reaction/1761091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
Reactant1,3-dimethyl-1H-indole-2-carbaldehydeHCID 2771468—
ReactantSodium cyanoborohydrideHCID 5003444—
Product(1,3-dimethyl-1H-indol-2-yl)-N-methylmethanamineHCID 2213913152%

Reaction Steps

To 1,3-dimethyl-1H-indole-2-carboxaldehyde (13.0 g, 75 mmole) was added a solution of 2.0 M methylamine in methanol (150 mL, 300 mmole) and HOAc (4.3 mL, 75 mmole). The solution was stirred at RT for 4 hr, then was cooled to 0° C. and sodium cyanoborohydride (5.0 g, 80 mmole) was added portionwise over 5 min. The reaction was then allowed to warm to RT. After 16 hr. the reaction was concentrated under vacuum and the residue was taken up in Et2O. The solution was washed with 1.0 N NaOH then with brine, dried (Na2SO4), and concentrated to dryness. Flash chromatography on silica gel (95:5 CHCl3/methanol containing 5% NH4OH) gave the title compound (7.34 g, 52%) as a yellow oil: 1H NMR (400 MHz, CDCl3) δ 7.53 (d, J=7.8 Hz, 1H), 7.26 (d, J=7.8 Hz, 1 H), 7.20 (t,1H), 7.09 (t,1H), 3.88 (s, 2H), 3.76 (s, 3H), 2.46 (s, 3H), 2.32 (s, 3H), 1.36 (br s,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-fecea52d09b440f6ac7ac5c7d7b52c15
Source noteuspto-grants-2005_01