HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21498552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,3,3-Trimethyl-2-azabicyclo[2.2.2]octan-5-ol | HCID 21498546 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21498552 | HCID 21498552 | 36.4% |
Reaction Steps
To a solution of 1.8 g (0.016 moles) of 1,3,3-trimethyl-2-azabicyclo[2.2.2]octane-5ol in 30 ml of glacial acetic acid in a 100 ml flask equipped with a magnetic stirrer, thermometer, condenser, and drying tube was added 1.0 ml (0.106 moles) of acetic anhydride. The solution was boiled under reflux for 20 hours. The reaction mixture was then cooled and evaporated under reduced pressure. The residue was taken up in hexane, and allowed to stand at room temperature overnight. The solution was then filtered and the filtrate evaporated under reduced pressure and dried under vacuum at 35° C, yielding 1.23 g of the desired material as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03991012 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-766a183fd5d74534b206f9f38d3b7579 |
| Source note | uspto-grants-1976_11 |