HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | Piperazine-2-carboxylic acid dihydrochloride | HCID 2723757 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid | HCID 5175855 | — |
Reaction Steps
piperazine-2-carboxylic acid dihydrochloride (10.0 g, 49.23 mmol) is dissolved in 1:1 dioxane/water (320 ml). 50% Aqueous sodium hydroxide is added to bring the pH to 11. BOC-ON (2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile), (15.59 g, 63.32 mmol) is dissolved in dioxane (80 ml) and added dropwise while maintaining the pH at 11 with 50% aqueous sodium hydroxide. The reaction is stirred overnight at ambient temperature. The reaction mixture is then extracted with diethyl ether (5×250 ml) and acidified to pH 2 with concentrated hydrochloric acid. The di-Boc compound is then extracted out with ethyl acetate (4×200 ml) and the acidic aqueous solution containing the desired mono-Boc product is then taken on in the synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138526B1 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-3719a34b138842879eede0a094e718f5 |
| Source note | uspto-grants-2006_11 |