HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N-(9-cyanobicyclo[3.3.1]non-9-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Water methylene chloride | HCID 21908982 | — |
| Reactant | 9-Aminobicyclo[3.3.1]nonane-9-carbonitrile | HCID 66720824 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(9-cyanobicyclo[3.3.1]non-9-yl)benzamide | HCID 66721238 | — |
Reaction Steps
Add a solution of 2.37 g (17.17 mmol) of potassium carbonate in 30 mL of water, then 1.37 mL (11.8 mmol) of benzoyl chloride, to a solution of 1.88 g (11.45 mmol) of 9-aminobicyclo[3.3.1]nonane-9-carbonitrile in 20 mL of THF. Stir the reaction mixture for 1 h at RT, then distribute in 100 mL of a 1:1 mixture of DCM/water. Wash the organic phase with 50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Solidify the residue obtained in 100 mL of pentane giving, after filtration and washing with pentane, 2.81 g of N-(9-cyanobicyclo[3.3.1]non-9-yl)benzamide in the form of white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552201B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-04462028245c4e4398c495e5996603eb |
| Source note | uspto-grants-2013_10 |