HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15790822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 15790818 | HCID 15790818 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15790822 | HCID 15790822 | — |
Reaction Steps
5 ml acetic anhydride is cooled to 0-5° C. and 2 drops boron trifluoride-etherate are added. Then 2.3 g (7.6 mmol) 1-(4-chlor-5-difluormethoxy-1-methyl-3-pyrazolyl)-5-formyl-4-pyrazol-carbonitrile is slowly added dropwise and stirring is continued for another 1.5 hours at room temperature. 9 ml of 10% sodium acetate solution is added, stirring is continued for 20 minutes at room temperature and then the mixture is shaken up with ethyl acetate. The combined ethyl acetate phases are washed with a solution of sodium hydrogen carbonate and sodium chloride, dried and concentrated. Purification is by column chromatography using a hexane/ethyl acetate mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06028034 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-b98ed92ff94942e98ca4655847427650 |
| Source note | uspto-grants-2000_02 |