Cyclopentyl chloroformate
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
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)
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
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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Cyclopentyl chloroformate(50715-28-1)Related Product Information
- Phenyl chlorothionocarbonate
- Phenyl chloroformate
- DI-N-PENTYL PHTHALATE-D4
- (+)-MENTHYL CHLOROFORMATE
- Dimethyl phthalate
- Benzyl chloroformate
- 4-Nitrobenzyl chloroformate
- Heptyl chloroformate
- 9-Fluorenylmethyl chloroformate
- Propyl chloroformate
- Isopropyl chloroformate
- Pentyl chloroformate
- Butyl chloroformate
- 2-Ethylhexyl chloroformate
- 2-CHLOROBENZYL CHLOROFORMATE
- 4-BROMOPHENYL CHLOROFORMATE
- 4-CHLOROPHENYL CHLOROFORMATE
- Cyclohexyl chloroformate