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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115196Generated: November 4, 2026

Acetic Acid → HCID 59813153, compound

https://huagongshe.com/reaction/2115196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 11471554HCID 11471554—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTrimethyl orthoformateHCID 9005—
ProductHCID 59813153HCID 59813153—

Reaction Steps

To 100 mg (355 μmol) of 3-(phenyl-thiophen-3-yl-methylene)-8-aza-bicyclo[3.2.1]octane in 1 mL of trimethyl orthoformate was added 62 μL (533 μmol) of 2-methylbenzaldehyde, 173 mg (817 μmol) of sodium triacetoxyborohydride, 34 μL of glacial acetic acid at room temperature. The reaction mixture was allowed to stir overnight at room temperature. Next day, the crude was diluted with 1 mL of dichloromethane and 0.5 mL of methanol. The diluted suspension was filtered and the precipitates were washed with dichloromethane. The combined filtrates were concentrated. The concentrated sample was purified by reverse phase chromatography (20×100 mm J'sphere H-80 YMC column using a gradient of 0.1% TFA/water to 5% water/0.1% TFA/acetonitrile). The eluent was evaporated to yield the title compound as a white solid; MS m/z (MH+) 386; 1H NMR 300 MHz (MeOD-d4) δ 6.86-7.51 (m, 12H), 4.26 (s, 2H), 4.05-4.11 (m, 2H), 2.03-2.89 (m, 11H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435822B2
Source datasetuspto-grants-2008_10
ORD IDord-7b5627222f3d433e94fa7c12da319fa6
Source noteuspto-grants-2008_10