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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167440Generated: October 31, 2026

Benzaldehyde → (Z)-tert-Butyl-7-(1-cyano-2-phenylvinyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

https://huagongshe.com/reaction/2167440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium ethoxideHCID 2723922—
Reactanttert-Butyl-7-(cyanomethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 66978184—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(Z)-tert-Butyl-7-(1-cyano-2-phenylvinyl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 6697813877%

Reaction Steps

To a solution of 0.231 mmol tert-butyl-7-(cyanomethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate in 2 ml ethanol were added 0.278 mmol of NaOEt solution (21%) and 0.254 mmol benzaldehyde. The mixture was stirred at room temperature over night. The mixture was diluted with ethanol and H2O, and a white precipitation observed. The solid was filtered off and washed with ethanol and H2O. The white solid was dissolved in methanol. Evaporation of the solvent gave 64 mg (77%) of solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045459B2
Source datasetuspto-grants-2015_06
ORD IDord-ce179c09b6b148219475ad9df97e73e2
Source noteuspto-grants-2015_06