HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-4-Bromo-beta-nitrostyrene → 1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-4-Bromo-beta-nitrostyrene | HCID 688204 | — |
| Reactant | 1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene | HCID 66629098 | — |
| Product | 1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzene | HCID 67064639 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722743B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-bc063512d9d74d9ca05e50fed697d0ea |
| Source note | uspto-grants-2014_05 |