ChemicalBook--->CAS DataBase List--->1000577-78-5

1000577-78-5

1000577-78-5 Structure

1000577-78-5 Structure
IdentificationBack Directory
[Name]

Tert-Butyl1-benzylazetidin-3-ylcarbamate
[CAS]

1000577-78-5
[Synonyms]

tert-Butyl (1-benzylazetidin-3-yl)
Tert-Butyl1-benzylazetidin-3-ylcarbamate
N-[1-(Phenylmethyl)-3-azetidinyl]carbamic acid tert-butyl ester
Carbamic acid, N-[1-(phenylmethyl)-3-azetidinyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C15H22N2O2
[MOL File]

1000577-78-5.mol
[Molecular Weight]

262.35
Chemical PropertiesBack Directory
[Boiling point ]

369.0±31.0 °C(Predicted)
[density ]

1.10
[storage temp. ]

2-8°C
[pka]

12.01±0.20(Predicted)
Hazard InformationBack Directory
[Synthesis]

tert-Butyl (azetidin-3-yl)carbamate hydrochloride

217806-26-3

Benzaldehyde

100-52-7

Tert-Butyl1-benzylazetidin-3-ylcarbamate

1000577-78-5

Tert-butyl azetidine-3-carbamate hydrochloride (200 mg, 0.96 mmol) and benzaldehyde (203 mg, 1.92 mmol) were added to triethylamine (0.133 mL, 0.96 mmol) and acetic acid (115 mg, 1.92 mmol) in methanol (10 mL), and the reaction was stirred for 30 min at 24 °C. Subsequently, sodium cyanoborohydride (181 mg, 2.88 mmol) was added to the reaction system. The reaction mixture was continued to be stirred at 24 °C for 12 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by column chromatography to afford tert-butyl (1-benzylazetidin-3-yl)carbamate (120 mg, 48% yield).LCMS (m/z): 262.2 [M + H]+.

[References]

[1] Patent: WO2015/200680, 2015, A2. Location in patent: Paragraph 00499
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