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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526447Generated: October 26, 2026

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → Tert-butyl 3-(cyclobutyl(methyl)amino)azetidine-1-carboxylate

https://huagongshe.com/reaction/526447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-MethylcyclobutanamineHCID 21830191—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-(cyclobutyl(methyl)amino)azetidine-1-carboxylateHCID 11760122648.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

Combined a solution of tert-butyl 3-oxoazetidine-1-carboxylate (500 mg, 2.92 mmol) and N-methylcyclobutanamine (0.373 mL, 3.50 mmol) in methylene chloride (15 mL) and added sodium triacetoxyborohydride (929 mg, 4.38 mmol) and the solution stirred at 20° C. for 3 h. The solution was concentrated in vacuo to give a white solid. The solid was taken up in ethyl acetate (50 mL), washed with saturated sodium bicarbonate (50 mL) and brine, dried with magnesium sulfate, and concentrated in vacuo to give a residue which was purified on a 40 g silica gel column eluted with 0 to 70% ethyl acetate in hexanes to give the title compound (342 mg, 1.423 mmol, 48.7%) as a clear, colorless oil. 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.43 (s, 9H) 1.60-1.75 (m, 2H) 1.85-2.04 (m, 4H) 2.07 (s, 3H) 2.81-2.94 (m, 1H) 3.27-3.30 (m, 1H) 3.81-3.88 (m, 2H) 3.88-3.97 (m, 2H); MS: 241 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-f9acd3fb045a45f0a23cb473376be451
Source noteuspto-grants-2016_05