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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694598Generated: October 31, 2026

Water → HCID 59156565, compound

https://huagongshe.com/reaction/1694598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl 4-nitrobenzylphosphonateHCID 256065—
ReactantHCID 86638343HCID 86638343—
Catalyst15-Crown-5HCID 36336—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59156565HCID 59156565101.5%

Reaction Steps

Sodium hydride (60% dispersion, 0.10 g, 2.6 mmol) and 15-crown-5 (0.038 g, 0.17 mmol) were added to THF (5 mL) at 0° C. and stirred for 5 min. To the reaction mixture was then added dropwise over 5 min a solution of diethyl (4-nitrobenzyl)phosphonate (0.52 g, 1.9 mmol) in THF (5 mL), and stirring was continued at 0° C. for 5 min. To this reaction mixture was then added dropwise over 10 min a solution of 74b (0.47 g, 1.7 mmol) in THF (10 mL). The reaction mixture was stirred for 30 min at 0° C. then for 90 min at RT. Water was carefully added, and the mixture was partitioned between water and EtOAc. The EtOAc layer was washed sequentially with water and brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified by SiO2 chromatography eluting with EtOAc/hexane to afford 0.67 g (94%) of 5-bromo-2-methoxy-1-(1-methylcyclopropyl)-3-[(E)-2-(4-nitrophenyl)vinyl]benzene (75) as a yellow solid (0.67 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158803B2
Source datasetuspto-grants-2012_04
ORD IDord-2eda3a1ef9a8408a8c392c0d0edaa376
Source noteuspto-grants-2012_04