HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21330481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21330334 | HCID 21330334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21330481 | HCID 21330481 | 42.8% |
Reaction Steps
To a solution of 2.5 g of 2,6-diethyl-1-(2-hydroxyethyl)-2,3,6-trimethyl-4-piperidyl benzoate (Compound 45 - prepared following the procedure described in Preparation 9) in 50 ml of dimethylformamide were added 2.0 g of triethylamine and 1 g of acetic anhydride; the mixture was then heated at 80° - 90° C for 5 hours. When the reaction was complete, the reaction mixture was concentrated and 50 ml of benzene were added. The mixture was then washed with, in turn, an aqueous solution of sodium carbonate and water, and was dried over anhydrous sodium sulphate. After removing the solvent, the residue was subjected to distillation under reduced pressure, giving 1.2 g of Compound 50 as a colourless oil (bp 195° C/0.008 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075165 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-78ef631ce16d414a95c6d390a2229eb5 |
| Source note | uspto-grants-1978_02 |