HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857916Generated: October 31, 2026
Hydrochloric Acid → 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid
https://huagongshe.com/reaction/857916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Piperazine-2-carboxylic acid dihydrochloride | HCID 2723757 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid | HCID 5175855 | — |
Reaction Steps
A mixture of piperazine-2-carboxylic acid dihydrochloride in dioxan (1000 ml) and water (500 ml), at 10–15° C., was treated with aqueous sodium hydroxide solution (50%) over 15 minutes to adjust the pH to 9.1. This mixture was then treated portionwise (0.1 equivalent portions) with tert-butyl dicarbonate (114.6 g) over a period of 1 hour whilst maintaining the temperature at 5° C. and the pH around 8.8. After stirring at room temperature overnight the reaction mixture was cooled to 10° C., then the pH of the mixture was adjusted to 2 by the addition of hydrochloric acid (37%) and then the mixture was concentrated at 40° C. under reduced pressure. The resulting solid was treated with methanol (1500 ml) and this mixture was heated at reflux temperature and then filtered to remove the insoluble inorganics. The filtrate was evaporated to give the title compound (126 g) as an off white solid. MS: 231 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07148215B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-11e7d116435b4cdcb0eb9d9c5d8f9986 |
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| Source note | uspto-grants-2006_12 |
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