Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Methyoxybenzoyl-N-glycine | HCID 128847 | — |
| Reactant | 1,4-Diazabicyclo(3.2.2)nonane | HCID 398407 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22243702 | HCID 22243702 | — |
Reaction Steps
0.42 g (2 mmol) of N-(4-methoxybenzoyl)glycine dissolved in 20 ml of dioxane is placed in a 50 ml round-bottomed flask, 0.45 g (2.2 mmol) of dicyclohexylcarbodiimide is added, the mixture is stirred at room temperature for 30 minutes, 0.25 g (2 mmol) of 1,4-diazabicyclo[3.2.2]nonane is added and the mixture is stirred for a further one hour. 20 ml of water are added, the precipitate formed is filtered off, the filtrate is extracted with chloroform, the organic phase is extracted with aqueous 0.1N hydrochloric acid solution and 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 |
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| Patent number | US07001902B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-beea767faf5d462a9846784031cefb0a |
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| Source note | uspto-grants-2006_02 |
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