Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526449Generated: October 27, 2026

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

https://huagongshe.com/reaction/526449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-methylcyclopropanamine hydrochlorideHCID 18546974—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-(cyclopropyl(methyl)amino)azetidine-1-carboxylateHCID 11760121155.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

Combined a solution of tert-butyl 3-oxoazetidine-1-carboxylate (175 mg, 1.022 mmol) and N-methylcyclopropanamine hydrochloride (121 mg, 1.124 mmol) in methylene chloride (5 mL) and added sodium triacetoxyborohydride (325 mg, 1.533 mmol) and the solution stirred at 20° C. for 30 min. The solution was concentrated in vacuo to give white solid which 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, and then purified on a 40 g silica gel column eluted with 0 to 50% ethyl acetate in hexanes to give the title compound (128 mg, 0.566 mmol, 55.3%) as a clear, colorless oil. MS: 227 (M+H). 1H NMR (400 MHz, METHANOL-d4) δ ppm 0.41-0.47 (m, 2H) 0.48-0.56 (m, 2H) 1.43 (s, 9H) 1.64 (tt, J=6.7, 3.9 Hz, 1H) 2.28 (s, 3H) 3.50 (tt, J=7.5, 5.7 Hz, 1H) 3.84-4.01 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-b98acfe955ea456681fbed935855a047
Source noteuspto-grants-2016_05