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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430810Generated: November 2, 2026

Acetic Acid → Benzyl 3-(4-methylpiperazin-1-yl)azetidine-1-carboxylate

https://huagongshe.com/reaction/1430810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantBenzyl 3-oxoazetidine-1-carboxylateHCID 10632047—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductBenzyl 3-(4-methylpiperazin-1-yl)azetidine-1-carboxylateHCID 86708494100.2%

Reaction Steps

A mixture of benzyl 3-oxoazetidine-1-carboxylate (1.026 g, 5 mmol), 1-methylpiperazine (0.833 mL, 7.50 mmol) and acetic acid (0.429 mL, 7.50 mmol) in 1,2-dichloroethane (5 mL) was stirred at room temperature for 3 h. sodium triacetoxyborohydride (2.119 g, 10.00 mmol) was added and the reaction mixture was stirred at room temperature overnight. A small amount of water was added to the reaction mixture and the reaction mixture was directly loaded onto a 120 g ISCO column and eluted with 1-12% 2N ammonia in methanol/dichloromethane). benzyl 3-(4-methylpiperazin-1-yl)azetidine-1-carboxylate (1.45 g) was obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940736B2
Source datasetuspto-grants-2015_01
ORD IDord-f64d3d7ff1ca47f39db761ca5fcf9eb5
Source noteuspto-grants-2015_01