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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374163Generated: October 31, 2026

Benzaldehyde → HCID 19734538, compound

https://huagongshe.com/reaction/374163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 19734488HCID 19734488—
SolventMethanolHCID 887—
ProductHCID 19734538HCID 1973453875%

Reaction Steps

N-cyano-N'-[2-(4-aminophenyl)ethyl]-3-pyridinecarboximidamide (0.20 g, 0.75 mmol) was dissolved in methanol (15 ml), and benzaldehyde (0.12 g, 1.13 mmol) and sodium cyanoborohydride (0.10 g, 1.59 mmol) were added. The mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residue thus obtained was extracted with chloroform (50 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (100:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.12 g, 0.34 mmol, yield: 75%) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166347
Source datasetuspto-grants-1992_11
ORD IDord-f5f05552b56142dd91a28a7c25179042
Source noteuspto-grants-1992_11