HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 6-[(4-Formylphenyl)(methyl)amino]hexyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | N-(6-Acetoxyhexyl)-N-methylaniline | HCID 19697246 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-[(4-Formylphenyl)(methyl)amino]hexyl acetate | HCID 15253979 | — |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
Phosphorous oxychloride (145 g, 0.95 mol) was added dropwise at 5° C. to 280 mL of stirred N,N-dimethylformamide (DMF), and the mixture was stirred at 5° C. for 2 hours. N-(6-Acetoxyhexyl)-N-methylaniline (230 g, 0.93 mol) was added slowly, and the reaction mixture was heated at 90° C. for 3 hours. After cooling, the solution was poured onto 500 g of ice and the resulting mixture was neutralized to pH 5 with sodium acetate. The mixture was extracted with dichloromethane (4×200 mL), the combined extracts were dried (MgSO4), and the solvent was removed at reduced pressure. The brown residue was distilled in vacuo the provide 186 g (73%) of a yellow oil, bp 195° C. (0.15 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792208 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-8c7c8fca8e834c4cbe6410ac068e4caf |
| Source note | uspto-grants-1988_12 |