HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethenyl-4-nitrobenzene → 1-Ethenyl-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethenyl-4-nitrobenzene | HCID 7481 | — |
| Reactant | 4-Nitrophenethyl bromide | HCID 79266 | — |
| Product | 1-Ethenyl-4-nitrobenzene | HCID 7481 | — |
| Product | (4-Nitrophenyl)acetaldehyde | HCID 11744988 | — |
Reaction Steps
p-Nitrophenylacetaldehyde was prepared by the method described in Lethbridge et al., J. Chem. Soc. Perkin I, 35 1973) from p-nitrophenylethylene. The p-nitrophenylethylene was prepared by the method described in Strassburg et al., J. Am. Chem. Soc. 69:2142 (1947) from 1-bromo-2-(p-nitrophenyl)ethane commercially obtainable from Aldrich Chemical Co., Milwaukee, Wis.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05187086 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-f684d861313c4ac480370e4c7a598173 |
| Source note | uspto-grants-1993_02 |