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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525952Generated: October 31, 2026

Acetic Acid → HCID 86732821, compound

https://huagongshe.com/reaction/525952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86732820HCID 86732820—
SolventDichloromethaneHCID 6344—
ProductHCID 86732821HCID 8673282141.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-ethyl-7,8-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinoline-3-carbaldehyde (10 g, 21.12 mmol) in Dichloromethane (DCM) (150 mL) was added pyrrolidine (2.61 mL, 31.7 mmol), sodium triacetoxyborohydride (8.95 g, 42.2 mmol) and AcOH (0.060 mL, 1.056 mmol). The reaction mixture was stirred at 25° C. for 3 h. LCMS showed completion of the reaction. The mixture was extracted with DCM and washed with brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. The crude material was purified by normal phase automatic silica column chromatography (Combiflash RF), using a 120 g column and eluting with MeOH/DCM (0-20%). The product was further purified with reverse phase automatic silica column chromatography (Combiflash RF), using a 150 g golden column and eluting with acetonitrile/water (0-60%) to afford 1-ethyl-7,8-bis((4-methoxybenzyl)oxy)-3-(pyrrolidin-1-ylmethyl)quinolin-4(1H)-one (4.6 g, 8.70 mmol, 41.2% yield) as a pale yellow solid. LCMS: (M+H)+: 529.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340556B2
Source datasetuspto-grants-2016_05
ORD IDord-e65c52dd64354b6ca2ccc21d333394b3
Source noteuspto-grants-2016_05