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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435557Generated: October 26, 2026

Acetic Acid → HCID 11703679, compound

https://huagongshe.com/reaction/1435557

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—
ProductHCID 11703679HCID 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)=384.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618650B2
Source datasetuspto-grants-2009_11
ORD IDord-efebb69552574c438f526672a796b3b5
Source noteuspto-grants-2009_11