Basic information Uses Safety Supplier Related

4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

Basic information Uses Safety Supplier Related

4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Basic information

Product Name:
4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
Synonyms:
  • N-BOC-HEXAHYDRO-1H-AZEPIN-4-OL
  • 1H-AZEPINE-1-CARBOXYLIC ACID, HEXAHYDRO-4-HYDROXY-, 1,1-DIMETHYLETHYL ESTER
  • 4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER, 95+%
  • 1-Boc-4-Hydroxyazepane
  • 4-hydroxy-1-azepanecarboxylic acid tert-butyl ester
  • 1-Boc-Hexahydro-1H-azepin-4-ol
  • 1-Boc-Hexahydro-1H-azepin...
CAS:
478832-21-2
MF:
C11H21NO3
MW:
215.29
Mol File:
478832-21-2.mol
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4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Chemical Properties

Boiling point:
310.6±35.0 °C(Predicted)
Density 
1.079±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
15.06±0.20(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN2811
HazardClass 
IRRITANT
HS Code 
2933998090
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4-HYDROXYAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Usage And Synthesis

Uses

4-Hydroxyazine-1-carboxylic acid tert-butyl ester is a carboxylic acid ester organic compound that can be used as a pharmaceutical intermediate.

Synthesis

39888-51-2

24424-99-5

478832-21-2

(c) Synthesis of tert-butyl 4-hydroxyazepane-1-carboxylate: Ammonium formate (900 mg) and 10% palladium/carbon catalyst (200 mg) were added to an ethanol solution (10 mL) of 1-benzyl-4-azepane (450 mg, 2.19 mmol), and the reaction mixture was heated and refluxed for 1 hour. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the filtrate was concentrated. The resulting residue was dissolved in dichloromethane (10 mL) and di-tert-butyl dicarbonate (0.504 mL, 2.19 mmol) was added at room temperature with continuous stirring for 19 hours. At the end of the reaction, saturated aqueous sodium bicarbonate solution was added to the mixture, followed by water and extraction with chloroform. The organic layers were combined, dried with anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=2/1) to afford the target compound tert-butyl 4-hydroxyazepane-1-carboxylate (333 mg, 70% yield).

References

[1] Patent: EP1500643, 2005, A1. Location in patent: Page 48

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