HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871061Generated: October 31, 2026
Sodium Hydroxide → 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid
https://huagongshe.com/reaction/871061
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
To a solution of 2-piperazine-carboxylic acid dihydrochloride (1.0 g, 4.92 mmol) in 20 mL of water/dioxane 1:1, NaOH 6N was added to adjust the pH to 11. A solution of BOC-ON (1.34 g, 5.41 mmol) in dioxane (5 mL) was then added dropwise, while maintaining the pH=11 during the addition and the resulting solution was stirred overnight at room temperature. Another 0.134 g of BOC-ON were added and the reaction mixture was stirred for 2 h. The solvent was evaporated under reduced pressure and the residue was diluted with diethyl ether/water (60 mL). The phases were separated and the pH of the aqueous layer was adjusted to 7 by slow addition of HCl 1N. Evaporation of water under reduced pressure afforded the title compound as a white solid which was dried in a vacuum oven at 50 C and used without further purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969573B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-f781459f7cf54478b07f241f796ac1a2 |
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| Source note | uspto-grants-2015_03 |
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