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| | 1-Chloroethyl (4-nitrophenyl) carbonate Basic information |
| Product Name: | 1-Chloroethyl (4-nitrophenyl) carbonate | | Synonyms: | Carbonic acid 4-nitro-phenyl ester 1-chloro-ethyl ester;1-Chloroethyl (4-nitrophenyl) carbonate;1-Chloroethyl p-nitrophenyl carbonate;Carbonic acid, 1-chloroethyl 4-nitrophenyl ester;Carbonic acid 1-chloro-ethyl ester 4-nitro-phenyl ester;Carbonic acid 4-nitro-phenyl ester 1-chloro-ethyl ester ISO 9001：2015 REACH;1-Chloroethyl-4-nitrophenyl carbonate (1-CENPC);1-Chloroethyl 4-nitrophenyl carbonat | | CAS: | 101623-69-2 | | MF: | C9H8ClNO5 | | MW: | 245.62 | | EINECS: | | | Product Categories: | | | Mol File: | 101623-69-2.mol |  |
| | 1-Chloroethyl (4-nitrophenyl) carbonate Chemical Properties |
| Melting point | 71.0-71.7 °C(Solv: hexane (110-54-3)) | | Boiling point | 359.1±42.0 °C(Predicted) | | density | 1.415±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | Appearance | White to light yellow Solid |
| | 1-Chloroethyl (4-nitrophenyl) carbonate Usage And Synthesis |
| Uses | A clear, colourless to pale yellow liquid used as an intermediate in Gabapentin, an API. | | Synthesis | To an ice cold reaction mixture containing p-nitrophenol (1.39 g, 10 mmol) and pyridine (0.81 g, 10 mmol) in dichloromethane (60 mL) was added 1-chloroethyl chloroformate (1.2 mL, 11 mmol). The mixture was stirred at 0° C for 30 min and then at room temperature for 1 hour. After removing the solvent under reduced pressure, the residue was dissolved in ether, washed with water, 10percent citric acid and water. The ether layer was dried over Na2SO4and evaporated under reduced pressure to give 2.4 g (97percent) of 1-Chloroethyl (4-nitrophenyl) carbonate as an off-white solid.
 | | References | [1] Journal of Antibiotics, 1999, vol. 52, # 7, p. 643 - 648
[2] Patent: US2006/229361, 2006, A1. Location in patent: Page/Page column 37
[3] Journal of Pharmacology and Experimental Therapeutics, 2016, vol. 357, # 2, p. 240 - 247
[4] Journal of Medicinal Chemistry, 1988, vol. 31, # 2, p. 318 - 322
[5] Patent: WO2011/92065, 2011, A1. Location in patent: Page/Page column 60 |
| | 1-Chloroethyl (4-nitrophenyl) carbonate Preparation Products And Raw materials |
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