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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921686Generated: October 25, 2026

Acetic Acid → (+/-) Tert-butyl 3-(hydroxymethyl)-4-(oxetan-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/921686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-OxetanoneHCID 15024254—
Reactant4-N-Boc-2-hydroxymethylpiperazineHCID 22386508—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(+/-) Tert-butyl 3-(hydroxymethyl)-4-(oxetan-3-yl)piperazine-1-carboxylateHCID 8670855662.1%

Reaction Steps

(+/−) Tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (3.07 g, 14.19 mmol), oxetan-3-one (1.820 mL, 28.4 mmol), AcOH (1.625 mL, 28.4 mmol), and 4 Å molecular sieves were taken up in DCM (16 mL) and MeOH (16.00 mL), and the reaction was stirred at room temperature overnight. Sodium cyanoborohydride (4.46 g, 71.0 mmol) was added and the reaction was stirred at room temperature for 2 h. The reaction mixture was filtered through celite, rinsing with MeOH. The solvent was removed in vacuo and the material was quenched with 2M K3PO4 solution, and then extracted 2× with EtOAc. The organic layers were combined, dried over Na2SO4, filtered, and concentrated. The material was purified by flash column chromatography (0-8% MeOH/DCM). (+/−) Tert-butyl 3-(hydroxymethyl)-4-(oxetan-3-yl)piperazine-1-carboxylate (2.40 g) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-3af88a335e03447396d0593d75988f7a
Source noteuspto-grants-2016_03