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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784359Generated: October 31, 2026

Triethylamine → HCID 86616768, compound

https://huagongshe.com/reaction/1784359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactantalpha-ChlorobenzylidenemalononitrileHCID 176977—
SolventEthanolHCID 702—
ProductHCID 86616768HCID 86616768—

Reaction Steps

Triethyl amine (1 ml) was added into a solution of N-Boc piperazine (1 g) and 2-(chloro(phenyl)methylene)malononitrile (1 g) in EtOH (20 ml). After 16 hours at 115° C., the reaction mixture was cooled down and some of desired product, tert-butyl 4-(2,2-dicyano-1-phenylvinyl)piperazine-1-carboxylate, precipitated out from the solution. After filteration, the mother solution was concentrated to offer a residue which was purified using silica gel chromatography to afford more tert-butyl 4-(2,2-dicyano-1-phenylvinyl)piperazine-1-carboxylate. 1H NMR (500 MHz, DMSO-d6) □7.53 (m, 5H), 3.93 (b, 2H), 3.61 (b, 2H), 3.36 (b, 2H), 3.15 (b, 2H), 1.39(s, 9H); 13C NMR(125 MHz, DMSO-d6) □170.9, 153.6, 132.6, 131.7, 129.1, 129.0, 117.4, 116.7, 79.4, 51.5, 50.33, 42.9, 27.9. MS m/z: (M+H)+ calcd for C19H23N4O2 339.18, found 339.17. Retention time 1.46 min (column A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504399B2
Source datasetuspto-grants-2009_03
ORD IDord-fa884b7c18a74d53a08928ef34d5e0f1
Source noteuspto-grants-2009_03