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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224705Generated: October 30, 2026

Benzaldehyde → HCID 11516025, compound

https://huagongshe.com/reaction/2224705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 59717864HCID 59717864—
SolventMethanolHCID 887—
ProductHCID 11516025HCID 1151602545.7%

Reaction Steps

Combine N-{4-[4-(2-amino-ethyl)-phenoxy]-phenyl}-acetamide (100 mg, 0.37 mmol), benzaldehyde (47 mg, 0.44 mmol), 3 Å molecular sieves (300 mg), and methanol (3 mL) and stir overnight at room temperature. Filter off the sieves then add sodium borohydride (28 mg) to the reaction and stirred at room temperature for 2 hours. Concentrate on a rotary evaporator and purified by radial chromatography on silica gel eluting with 10% conc. ammonium hydroxide in ethanol and chloroform to yield N-{4-[4-(2-benzylamino-ethyl)-phenoxy]-phenyl}-acetamide, (61 mg): 1H NMR (CDCl3, 300.00 MHz): 7.51-6.88 (m, 13H), 3.84 (s, 2H), 2.97-2.78 (m, 4H), 2.21 (s, 3H), 1.55 (s, 1H); HPLC=99% (5/95 to 95/5 ACN/(0.1% TFA in water) over 10 minutes, Zorbax SB-Phenyl 4.6 mm×15 cm×5 micron, λ=254 nM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378448B2
Source datasetuspto-grants-2008_05
ORD IDord-cc45883c84d649218a77079da4cedda1
Source noteuspto-grants-2008_05