HuagongsheHuagongshe Chemistry Print Report · For research reference only
9-Benzoylamino bicyclo[3.3.1]nonane-9-carboxylic acid → 9-aminobicyclo[3.3.1]nonane-9-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9-Benzoylamino bicyclo[3.3.1]nonane-9-carboxylic acid | HCID 66720767 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 9-aminobicyclo[3.3.1]nonane-9-carboxylic Acid | HCID 4866632 | 98.3% |
Reaction Steps
Dissolve 3 g (10.44 mmol) of 9-benzoylamino bicyclo[3.3.1]nonane-9-carboxylic acid in 200 mL of AcOH and 50 mL of 6N HCl aqueous solution, reflux the mixture for 18 h and then concentrate partially by distillation of 150 mL of solvent. After cooling, filter the reaction mixture and distribute in 150 mL of a 1:2 mixture of 1N HCl aqueous solution/ether. After extraction, concentrate the aqueous phase and then treat it dropwise with a 12N aqueous solution of soda (NaOH) to adjust the pH to 5-6. Filter the amino acid thus precipitated, wash with 3×50 mL of water and dry under reduced pressure, which gives 1.88 g of 9-aminobicyclo[3.3.1]nonane-9-carboxylic acid in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552201B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-3e10d4f716024efea54bfb66ce65614b |
| Source note | uspto-grants-2013_10 |