tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate

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tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate Basic information
Product Name:tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate
Synonyms:4-(2-Fluoro-4-nitrophenyl)piperazine, N1-BOC protected;tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate;1-Boc-4-(2-Fluoro-4-nitrophenyl)piperazine, 97%;3-Fluoro-4-[4-(tert-butoxycarbonyl)piperazin-1-yl]nitrobenzene;1-Piperazinecarboxylic acid, 4-(2-fluoro-4-nitrophenyl)-, 1,1-dimethylethyl ester;1-Boc-4-(2-Fluoro-4-nitrophenyl)piperazine,97%;1-boc-4-(2-fluoro-4-nitrophenyl)piperazine
CAS:154590-34-8
MF:C15H20FN3O4
MW:325.34
EINECS:
Product Categories:
Mol File:154590-34-8.mol
tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate Structure
tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate Chemical Properties
Melting point 153-155 °C(Solv: ethyl ether (60-29-7))
Boiling point 453.5±45.0 °C(Predicted)
density 1.270±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form Solid
pka0.11±0.10(Predicted)
AppearanceLight yellow to yellow Solid
CAS DataBase Reference154590-34-8
Safety Information
HS Code 2933599590
MSDS Information
tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate Usage And Synthesis
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

1-(2-Fluoro-4-nitrophenyl)piperazine

154590-33-7

tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate

154590-34-8

General procedure for the synthesis of tert-butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate: 1. 1-(2-fluoro-4-nitrophenyl)piperazine (12.5 g, 55.8 mmol) was dissolved in 1,4-dioxane (108 mL) under cooling conditions in an ice bath. 2. 1N sodium hydroxide solution (54 mL) and di-tert-butyl dicarbonate (14 mL, 61.38 mmol) were added sequentially to the above solution. 3. The temperature of the reaction mixture was adjusted to 25-35°C and stirred continuously for 0.5 hours. 4. Upon completion of the reaction, the mixture was poured into ice-cold water (200 mL) and a yellow precipitate was precipitated. 5. The precipitate was collected by filtration through a Büchner funnel to afford the target product tert-butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate (18.0 g, 99% yield). Product characterization data: 1H NMR (CDCl3): δ 8.01-7.88 (m, 2H), 6.93 (t, J = 8.6 Hz, 1H), 3.61 (t, J = 4.9 Hz, 4H), 3.24 (t, J = 4.9 Hz, 4H), 1.49 (s, 9H). IR (KBr, cm-1): 3119, 1692, 1605, 1512. CI-MS (m/z): 326 (M++1), 270, 240, 226, 195, 183, 131, 96.

References[1] Patent: WO2005/82892, 2005, A2. Location in patent: Page/Page column 61
[2] Patent: CN107033095, 2017, A. Location in patent: Paragraph 0085; 0086
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 19, p. 4261 - 4267
[4] Patent: US2004/220194, 2004, A1. Location in patent: Page 13; 14
[5] Patent: US2005/239795, 2005, A1. Location in patent: Page/Page column 18
tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate Preparation Products And Raw materials
Raw materialsDi-tert-butyl dicarbonate-->3,4-Difluoronitrobenzene-->1-BOC-Piperazine-->1-(2-Fluoro-4-nitrophenyl)piperazine-->1,4-Dioxane-->Water-->Sodium hydroxide
Preparation Products1-(2-Fluoro-4-nitrophenyl)piperazine
Tag:tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate(154590-34-8) Related Product Information
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