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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038560Generated: October 31, 2026

Formic Acid → (2S,5R)-1-Boc-2,5-dimethylpiperazine

https://huagongshe.com/reaction/1038560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
Reactant(2S,5R)-4-Benzyl-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl esterHCID 66598992—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product(2S,5R)-1-Boc-2,5-dimethylpiperazineHCID 11745988101.1%

Reaction Steps

(2S,5R)-tert-butyl 4-benzyl-2,5-dimethylpiperazine-1-carboxylate (3.11 g, 10.2 mmol) was dissolved in methanol (19 mL), added palladium carbon (156 mg) under an argon atmosphere, and added formic acid (2.4 g, 51.1 mmol) under ice-cold conditions. The solution was reverted to room temperature, and stirred overnight. Then, the reaction solution was filtered through a pad of celite, and the filtrate was concentrated in vacuo. The obtained residue was added water and hexane, and extracted. An aqueous solution of sodium hydroxide was added to the aqueous layer, extracted with 2-methyltetrahydrofuran, dried over anhydrous sodium sulfate, concentrated in vacuo, and the title compound (2.21 g (yield >100%)) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551985B2
Source datasetuspto-grants-2013_10
ORD IDord-7ef19673402e4c90b27aeb4de2f175a9
Source noteuspto-grants-2013_10