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Cyclopentyl chloroformate

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Cyclopentyl chloroformate Basic information

Product Name:
Cyclopentyl chloroformate
Synonyms:
  • CYCLOPENTYL CHLOROFORMATE
  • CARBONOCHLORIDIC ACID, CYCLOPENTYL ESTER
  • Cyclopentyl carbonochloridoate
  • Cyclopentyl carbonochloridate
  • Cyclopentyl carbonochloridoate, [(Chlorocarbonyl)oxy]cyclopentane, [(Chloroformyl)oxy]cyclopentane
  • yclopentyl chloroformate
CAS:
50715-28-1
MF:
C6H9ClO2
MW:
148.59
EINECS:
411-460-0
Product Categories:
  • CHLOROFORMATES
  • Ring Systems
Mol File:
50715-28-1.mol
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Cyclopentyl chloroformate Chemical Properties

Boiling point:
69.0-70.5 °C(Press: 25 Torr)
Density 
1.19±0.1 g/cm3(Predicted)
form 
liquid
color 
Brown
InChI
InChI=1S/C6H9ClO2/c7-6(8)9-5-3-1-2-4-5/h5H,1-4H2
InChIKey
ZFQCRLNKHHXELH-UHFFFAOYSA-N
SMILES
C(Cl)(OC1CCCC1)=O
CAS DataBase Reference
50715-28-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
10-22-23-41-43-48/22
Safety Statements 
26-36/37/39-45
RIDADR 
UN3277
Hazard Note 
Irritant
HazardClass 
6.1, 8
HS Code 
2916200090
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Cyclopentyl chloroformate Usage And Synthesis

Uses

Cyclopentyl Chloroformate is a chemical reagent used in the synthesis of novel peptidomimetic Hep C protease inhibitors.

Synthesis

32315-10-9

96-41-3

50715-28-1

A mixed solution of cyclopentanol (10.9 mL, 120 mmol) and pyridine (10.7 mL, 132 mmol) was added slowly and dropwise to a solution of triphosgene (11.87 g, 40.0 mmol) in anhydrous ether (100 mL) at -70 °C. The reaction mixture was stirred continuously for 1 h at this temperature and then removed from the low temperature bath. Stirring was continued at room temperature for 1.5 h. Subsequently, 1.0 N HCl aqueous solution (110 mL) was added for acidification. The organic phase was separated, washed with brine (60 mL) and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to afford cyclopentyl chloroformate (14.395 g, boiling point 80 °C/75 mmHg, 80.7% yield). The resulting cyclopentyl chloroformate could be used directly in the subsequent reaction without further purification.

References

[1] Patent: CN106045802, 2016, A. Location in patent: Paragraph 0044-0045
[2] Patent: WO2008/95058, 2008, A1. Location in patent: Page/Page column 31
[3] European Journal of Medicinal Chemistry, 1993, vol. 28, # 1, p. 37 - 45
[4] Patent: WO2008/38175, 2008, A2. Location in patent: Page/Page column 38
[5] Patent: CN107417748, 2017, A. Location in patent: Paragraph 0106

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