Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053981Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → (E)-3-{1-[5-Chloro-2-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-acrylic acid methyl ester

https://huagongshe.com/reaction/1053981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantLithium ChlorideHCID 433294—
ReactantTrimethylphosphonoacetateHCID 53413272—
Reactant1-[5-Chloro-2-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazole-3-carbaldehydeHCID 86685689—
SolventAcetonitrileHCID 6342—
Product(E)-3-{1-[5-Chloro-2-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-acrylic acid methyl esterHCID 68019133—

Reaction Steps

A solution of aldehyde 5 (0.25 g, 0.65 mmol), LiCl (0.03 g, 1.21 mmol), trimethylphosphonoacetate (0.11 mL, 0.71 mmol) and DBU (0.19 mL, 1.21 mmol) in CH3CN (10 mL) was stirred under a N2 atmosphere at RT for 2 h. The reaction mixture was partitioned between 2 M HCl (15 mL) and EtOAc (20 mL). The organic layer was separated, washed with sat. NaHCO3 (15 mL), brine (15 mL), dried (Na2SO4) and the volatiles were removed in vacuo to give a crude ester 6, 0.31 g (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394284B2
Source datasetuspto-grants-2016_07
ORD IDord-b0126dfb271941899deb680e00948410
Source noteuspto-grants-2016_07