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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492921Generated: October 28, 2026

Acetic Acid → HCID 23153085, compound

https://huagongshe.com/reaction/492921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23153085HCID 2315308558.3%

Reaction Steps

To 1-Boc-azetidin-3-on (1.00 g) and 4-(tert-butoxycarbonylamino)piperidine (1.17 g) dissolved in methanol (50 ml) were added acetic acid (0.368 ml) and 10% palladium carbon (1.0 g), followed by stirring under hydrogen atmosphere at room temperature for 12 hours. The reaction mixture was stirred under hydrogen atmosphere (0.4 MPa) at room temperature for 4 hours. The reaction mixture was filtered to remove the catalyst. The filtrate was concentrated under reduced pressure. Ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate were added thereto, followed by partition. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated. The resultant crystals were suspended in diethyl ether-hexane, collected by filtration, and washed with hexane. There crystals were dried under aeration to provide the title compound (1.21 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-fcc44757a282443e88daf1aa5057543e
Source noteuspto-grants-2009_05