HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21545529, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21545531 | HCID 21545531 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21545529 | HCID 21545529 | — |
Reaction Steps
Two grams of 1-(2-carbamoylmethylphenoxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl]propan-2-ol are added to 20 ml. of anhydrous pyridine, followed by the immediate addition of 8.0 g. of acetic anhydride with stirring. The resulting solution is refluxed for a period of 5 minutes, cooled and subsequently poured into 50 ml. of ice water, basified with 2N aqueous sodium hydroxide solution and extracted with chloroform. The organic phase is then washed with water, dried over anhydrous sodium sulfate and evaporated to yield the crude product. After recrystallization from ethanol, there is obtained pure 1-(2-carbamoylmethylphenoxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl]-2-acetoxypropane as final product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951983 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-d2cf97a576394c3491735d8d8bab1f39 |
| Source note | uspto-grants-1976_04 |