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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746086Generated: October 26, 2026

trans-4-Bromo-beta-nitrostyrene → 1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzene

https://huagongshe.com/reaction/1746086

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-4-Bromo-beta-nitrostyreneHCID 688204—
Reactant1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzeneHCID 66629098—
Product1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzeneHCID 6706463927%

Reaction Steps

This compound was synthesized using the same methodology described in Intermediate C, using the commercially available (E)-1-bromo-4-(2-nitrovinyl)benzene as starting material. Yield: 27%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149447B2
Source datasetuspto-grants-2015_10
ORD IDord-85b300520a914e329fd989200b61832d
Source noteuspto-grants-2015_10