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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931512Generated: November 4, 2026

Acetic Acid → HCID 44219032, compound

https://huagongshe.com/reaction/1931512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68628477HCID 68628477—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 44219032HCID 4421903255.3%

Reaction Steps

A solution of (6-aminomethyl-quinolin-2-yl)-(R)-indan-1-yl-amine (example 54, step A) (130 mg, 0.45 mmol), 4-fluorobenzaldehyde (61 mg, 0.49 mmol) and acetic acid (108 mg, 1.8 mmol) in 1,2-dichloroethane (5 ml) was stirred at room temperature for 30 min. Afterwards sodium triacetoxy-borohydride (222 mg, 0.94 mmol) was added, the reaction mixture was allowed to stir for 2.5 days at room temperature, poured into ice/saturated sodium bicarbonate solution (30 ml) and extracted with dichloromethane (2×40 ml). The combined organic layers were washed with brine (30 ml), dried (MgSO4) and evaporated. The crude product was purified by flash chromatography (ethyl acetate/heptane) on silica gel to yield the title compound as a colorless oil (99 mg, 55%). MS: m/e=398.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188284B2
Source datasetuspto-grants-2012_05
ORD IDord-7fc47502e1784d939d490c07ad9b4c1d
Source noteuspto-grants-2012_05