5-Fluoro-1,3-dihydro-benzimidazol-2-one

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5-Fluoro-1,3-dihydro-benzimidazol-2-one manufacturers

5-Fluoro-1,3-dihydro-benzimidazol-2-one Basic information
Product Name:5-Fluoro-1,3-dihydro-benzimidazol-2-one
Synonyms:5-FLUORO-1,3-DIHYDROBENZOIMIDAZOL-2-ONE, 95+%;5-Fluoro-1,3-dihydrobenzoimidazol-2-one;5-fluoro-1,3-dihydro-2H-benzimidazol-2-one;2H-BenziMidazol-2-one, 5-fluoro-1,3-dihydro-;5-Fluoro-1H-benzo[d]iMidazol-2(3H)-one;5-Fluoro-1H-benzo[d]imidazol-2(3H);5-FLUOROBENZIMIDAZOLONE;2H-Benzimidazol-2-one,5-fluoro-1,3-dihydro-(9CI)
CAS:1544-75-8
MF:C7H5FN2O
MW:152.13
EINECS:200-258-5
Product Categories:BENZIMIDAZOLE
Mol File:1544-75-8.mol
5-Fluoro-1,3-dihydro-benzimidazol-2-one Structure
5-Fluoro-1,3-dihydro-benzimidazol-2-one Chemical Properties
Melting point 300 °C
Boiling point 118.8±19.0 °C(Predicted)
density 1.366±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka11.00±0.30(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933998090
MSDS Information
5-Fluoro-1,3-dihydro-benzimidazol-2-one Usage And Synthesis
Synthesis
Carbon dioxide

124-38-9

3,4-Diaminofluorobenzene

367-31-7

5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE

1544-75-8

The general procedure for the synthesis of 5-fluoro-1H-benzo[d]imidazol-2(3H)-ones from carbon dioxide and 4-fluoro-1,2-benzenediamine was as follows: 4-fluoro-1,2-benzenediamine (1 mmol), Catalyst I (0.15 mmol), and N-methylpyrrolidone (NMP, 1 mL) were added in a Schlenk tube and placed in a magnetic stirrer. Carbon dioxide (1 atm) was passed into the reaction system via a balloon and the reaction mixture was subsequently stirred at 140 °C for 24 hours. The reaction progress was monitored periodically by GC, LC, GC-MS or NMR. For the reaction under high pressure conditions, the reaction was carried out by placing the reactants in a Teflon vessel and then in a stainless steel autoclave and passing carbon dioxide up to 20 atm.

References[1] Angewandte Chemie - International Edition, 2012, vol. 51, # 27, p. 6700 - 6703
[2] Chemistry - An Asian Journal, 2016, vol. 11, # 19, p. 2735 - 2740
[3] ACS Catalysis, 2013, vol. 3, # 9, p. 2076 - 2082
[4] Catalysis Today, 2014, vol. 226, p. 160 - 166
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