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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535791Generated: October 25, 2026

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

https://huagongshe.com/reaction/535791

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 1-bromo-4-[(trans)-2-nitrovinyl]benzene as starting material. 27% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859555B2
Source datasetuspto-grants-2014_10
ORD IDord-6fc97fe0b98d4b739dec6f4b7a7f1b41
Source noteuspto-grants-2014_10