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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157320Generated: November 1, 2026

Benzaldehyde → HCID 68691357, compound

https://huagongshe.com/reaction/1157320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-(cyanomethyl)piperazine-1-carboxylateHCID 21936030—
SolventDimethylformamideHCID 6228—
ProductHCID 68691357HCID 68691357—

Reaction Steps

To sodium hydride (0.1 g) taken in dry DMF (5 ml), under nitrogen, compound tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate (0.5 g) was added and allowed to stir at room temperature for half an hour. Benzaldehyde (280 mg) was added to the above reaction mixture and allowed to stir for 3 hours at room temperature. The reaction mixture was quenched with ice water (50 ml) and extracted with ethyl acetate (3×10 ml). The combined organic layer was washed with brine (10 ml), dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by column chromatography using MeOH: CH2Cl2 (0.5:9.5) as an eluent to afford tert-butyl 4-(1-cyano-2-phenylvinyl)piperazine-1-carboxylate as pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-b0907b4d64b446efbd0194792cf4edbf
Source noteuspto-grants-2010_10