Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864771Generated: October 27, 2026

Acetic Acid → N-Benzyl-N-[3-(1H-indol-5-yl)-benzyl]-N',N'-dimethyl-ethane-1,2-diamine

https://huagongshe.com/reaction/1864771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,2-Ethanediamine, N1,N1-dimethyl-N2-(phenylmethyl)-HCID 66029—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(1H-indol-5-yl)benzaldehydeHCID 4135879—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Benzyl-N-[3-(1H-indol-5-yl)-benzyl]-N',N'-dimethyl-ethane-1,2-diamineHCID 1170367968.7%

Reaction Steps

Sodium triacetoxyborohydride (480 mg, 2.3 mmol) was added to a solution of 3-(1H-indol-5-yl)-benzaldehyde (250 mg, 1.1 mmol) and N′-benzyl-N,N-dimethyl-ethane-1,2-diamine (600 mg, 3.4 mmol) and acetic acid (204 mg, 3.4 mmol) in 8 mL of tetrahydrofuran. The mixture was stirred at ambient temperature overnight, and then it was diluted with ethyl acetate, and neutralized with the careful addition of saturated sodium bicarbonate solution. The layers were separated and the organic phase was treated with polystyrene supported isocyanate resin (1.49 mmol/g, 1.7 g) for 2 h. The mixture was filtered and the filtrate was washed with 1M sodium carbonate solution. The aqueous phase was extracted into ethyl acetate, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated to leave 290 mg of the title compound. LC/MS (short method): retention time, 2.61 min; (M+H)=384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625889B2
Source datasetuspto-grants-2009_12
ORD IDord-813e7f882bc94dbcb52d3fdb73d860b2
Source noteuspto-grants-2009_12