Basic information Uses Safety Supplier Related

1-Boc-azetidine-2-carboxylic acid methyl ester

Basic information Uses Safety Supplier Related

1-Boc-azetidine-2-carboxylic acid methyl ester Basic information

Product Name:
1-Boc-azetidine-2-carboxylic acid methyl ester
Synonyms:
  • Methyl N-Boc-Azetidine-2-carboxylate
  • 1-Boc-Azetidine-2-carboxy...
  • Methyl 1-Boc-azetidine-2-carboxylate
  • 1,2-Azetidinedicarboxylic acid, 1-(1,1-dimethylethyl) 2-methyl ester
  • O1-tert-Butyl O2-methyl azetidine-1,2-dicarboxylate
  • 1-O-tert-butyl 2-O-methyl azetidine-1,2-dicarboxylate
  • tert-butyl methyl azetidine-1,2-dicarboxylate
  • 1-TERT-BUTYL METHYL AZETIDINE-1,2-DICARBOXYLATE
CAS:
255882-72-5
MF:
C10H17NO4
MW:
215.25
Mol File:
255882-72-5.mol
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1-Boc-azetidine-2-carboxylic acid methyl ester Chemical Properties

Boiling point:
269.0±33.0 °C(Predicted)
Density 
1.152±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-3.46±0.40(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

HS Code 
2933998090
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1-Boc-azetidine-2-carboxylic acid methyl ester Usage And Synthesis

Uses

Azacyclic butane-2-carboxylic acid has been used in the preparation of many inhibitors, such as liver fibrosis inhibitors and algal growth inhibitors. Furthermore, azacyclic butane-2-carboxylic acid also has important applications in many asymmetric synthetic fields.

Synthesis

67-56-1

159749-28-7

255882-72-5

Isobutyl chloroformate (8.43 g, 61.7 mmol) was slowly added to a solution of anhydrous THF (20 mL) containing N-Boc-azetidine-2-carboxylic acid (12.42 g, 61.7 mmol) and N-methylmorpholine (6.23 g, 61.7 mmol) under nitrogen protection, and the rate of addition was controlled to maintain a reaction temperature of less than -8 °C. After addition, the reaction mixture was stirred at -8 °C for 1 hour, then brought to room temperature and continued stirring for 3 hours. Methanol (200 mL) was added to the reaction solution and stirred at room temperature for 18 hours. Upon completion of the reaction, the volatile components were removed by distillation under reduced pressure and the residue was partitioned with water and diethyl ether. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the oily product methyl N-Boc-2-azetidinecarboxylate (11.15 g, 84.0% yield). The product was confirmed by NMR hydrogen spectrum (CDCl3): δ 1.43 (s, 9H), 2.20 (m, 1H), 2.50 (m, 1H), 3.78 (s, 3H), 3.90 (m, 1H), 4.00 (m, 1H), 4.60 (m, 1H).

References

[1] Patent: WO2006/100461, 2006, A1. Location in patent: Page/Page column 79

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