Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1,4-Diazabicyclo(3.2.2)nonane | HCID 398407 | — |
| Reactant | HCID 787887 | HCID 787887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22243705 | HCID 22243705 | — |
Reaction Steps
0.77 g (3 mmol) of N-(3-bromobenzoyl)glycine dissolved in 30 ml of dioxane is placed in a 100 ml round-bottomed flask, 0.68 g (3.3 mmol) of dicyclohexylcarbodiimide is added and the mixture is stirred at room temperature for 30 minutes, 0.38 g (3 mmol) of 1,4-diazabicyclo[3.2.2]nonane is added and the mixture is stirred for a further two hours. 30 ml of water are added and the precipitate formed is filtered off, the filtrate is extracted with chloroform and the organic phase is then extracted with aqueous 0.1N hydrochloric acid solution. The aqueous extraction phase is basified to pH 10 by addition of concentrated aqueous sodium hydroxide solution and extracted with chloroform. The organic phase is dried over sodium sulfate and concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07001902B2 |
|---|
| Source dataset | uspto-grants-2006_02 |
|---|
| ORD ID | ord-f2d88539f56744cf878648270df29abd |
|---|
| Source note | uspto-grants-2006_02 |
|---|