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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669719Generated: October 30, 2026

Acetic Acid → {2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanol

https://huagongshe.com/reaction/1669719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinoline-5-carbaldehydeHCID 86619493—
Solvent1,1-DichloroethaneHCID 6365—
Product{2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanolHCID 44218152—

Reaction Steps

2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinoline-5-carbaldehyde (150 mg, 0.56 mmol) was dissolved in 5 mL dichloroethan. Acetic acid (136 mg, 2.3 mmol) and sodium triacetoxy borohydride (258 mg, 1.2 mmol) were added. The reaction mixture was stirred at room temperature overnight and quenched by addition of 2N sodium carbonate solution (50 mL). The mixture was extracted three times with ethyl acetate (100 mL each). The organic phases were pooled, dried with sodium sulfate, filtered and evaporated. The residue was purified by flash chromatography on silica gel (heptane/ethyl acetate 100:0->50:50 gradient). The title compound was obtained as a light brown solid (105 mg, 69%), MS: m/e=269.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989628B2
Source datasetuspto-grants-2011_08
ORD IDord-e635a2a9f43f464a90b0ecf7c801b485
Source noteuspto-grants-2011_08