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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-Methylcyclobutanamine | HCID 21830191 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 3-(cyclobutyl(methyl)amino)azetidine-1-carboxylate | HCID 117601226 | 48.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345713B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-f9acd3fb045a45f0a23cb473376be451 |
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| Source note | uspto-grants-2016_05 |
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