HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Vinylbenzaldehyde → 4-Vinylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Vinylbenzaldehyde | HCID 39389 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Vinylbenzaldehyde | HCID 39389 | — |
| Product | Benzaldehyde, 2-ethenyl- | HCID 39391 | — |
Reaction Steps
Aldehyde 11 was synthesized by radical addition (Lub et al. (1997) Liebigs Ann. Recueil, 2281–2288) of thioacetic acid to 4-vinylbenzaldehyde. Vinyl benzaldehyde was synthesized by the procedure of Ren et al. (1993) Bull. Chem. Soc. Jpn. 66: 1897–1902 with the following changes: The addition of DMF was performed at a 38 mmol scale at 0° C. Purification by column chromatography (silica, Et2O/hexanes, 1:3) afforded 4-vinylbenzaldehyde in 60% yield (FIG. 37).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07042755B1 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-7634c165a21d451eaed7b282210961fa |
| Source note | uspto-grants-2006_05 |