HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vanillin → 4-[1-(4-Chloro-phenyl)-ethoxy]-3-methoxy-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | p-Chlorophenethylic alcohol | HCID 74647 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[1-(4-Chloro-phenyl)-ethoxy]-3-methoxy-benzaldehyde | HCID 58086817 | — |
Reaction Steps
4-Chlorophenylmethylcarbinol (643, 0.668 mL, 6.57 mmol) was dissolved in tetrahydrofuran (60.0 mL) at 0° C. under an atmosphere of nitrogen. 4-Hydroxy-3-methoxybenzaldehyde (105, 1.00 g, 6.57 mmol) and triphenylphosphine (2.07 g, 7.89 mmol) were added to the reaction, followed by diisopropyl azodicarboxylate (1.55 mL, 7.89 mmol) over 10 minutes. The reaction was stirred for 2 hours. The mixture was adsorbed onto silica and purified by silica gel chromatography, ethyl acetate:hexanes, to provide the desired compound, (644, 1.14 g, 60%). 1H-NMR was consistent with the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470818B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-86bb91da8fa84323a8bc104e135deac1 |
| Source note | uspto-grants-2013_06 |