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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantPiperazine-2-carboxylic acid dihydrochlorideHCID 2723757—
ReactantTert-butyldicarbonateHCID 22064466—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acidHCID 5175855—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148215B2
Source datasetuspto-grants-2006_12
ORD IDord-11e7d116435b4cdcb0eb9d9c5d8f9986
Source noteuspto-grants-2006_12