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2,7-DibroMo-9,9-difluoro-9H-fluorene

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CAS:1229603-71-7
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CAS:1229603-71-7
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Products Intro: Product Name:2,7-DibroMo-9,9-difluoro-9H-fluorene
CAS:1229603-71-7
Purity:98% Package:1G;10G;1KG,5KG,10KG

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2,7-DibroMo-9,9-difluoro-9H-fluorene Basic information
Product Name:2,7-DibroMo-9,9-difluoro-9H-fluorene
Synonyms:2,7-DibroMo-9,9-difluoro-9H-fluorene;9H-Fluorene, 2,7-dibroMo-9,9-difluoro-;2,7-Dibromo-9,9-difluorofluorene
CAS:1229603-71-7
MF:C13H6Br2F2
MW:359.99
EINECS:
Product Categories:
Mol File:1229603-71-7.mol
2,7-DibroMo-9,9-difluoro-9H-fluorene Structure
2,7-DibroMo-9,9-difluoro-9H-fluorene Chemical Properties
Melting point 138.0 to 142.0 °C
Boiling point 361.5±42.0 °C(Predicted)
density 1.95±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Light yellow to Light orange
Safety Information
HS Code 2903.99.8001
MSDS Information
2,7-DibroMo-9,9-difluoro-9H-fluorene Usage And Synthesis
Synthesis
2,7-Dibromo-9H-fluoren-9-one

14348-75-5

2,7-DibroMo-9,9-difluoro-9H-fluorene

1229603-71-7

The general procedure for the synthesis of 2,7-dibromo-9,9-difluoro-9H-fluorene from 2,7-dibromo-9-fluorenone is as follows: 2,7-dibromo-9-fluorenone (4.0 g, 11.8 mmol) was suspended in deoxyfluoric acid (12 mL) at room temperature and ethanol (4 drops) was added. The stirred suspension was heated at 90 °C for 24 h. (Note: when using deoxyfluor at high temperatures, a rapid and violent exothermic reaction may occur). When the reaction is complete, the mixture is cooled to room temperature and poured onto ice containing sodium bicarbonate. The solid formed is collected by filtration. The crude product was dissolved in ethyl acetate and washed sequentially with 1 M aqueous hydrochloric acid and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and the solvent evaporated to give the crude product. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford the target product 2,7-dibromo-9,9-difluoro-9H-fluorene (3.2 g).19F-NMR (282 MHz, dmso-d6) δ: -111.6 ppm.The solution of the product in ethyl acetate was passed through activated charcoal prior to the next step in the use.

References[1] Patent: WO2013/22810, 2013, A1. Location in patent: Page/Page column 22
[2] Patent: WO2013/28953, 2013, A1. Location in patent: Page/Page column 70-71
[3] Patent: WO2013/98313, 2013, A1
[4] Patent: WO2013/40492, 2013, A2. Location in patent: Page/Page column 88-89
[5] Patent: US2013/273005, 2013, A1. Location in patent: Paragraph 0342
2,7-DibroMo-9,9-difluoro-9H-fluorene Preparation Products And Raw materials
Raw materials2,7-Dibromo-9H-fluoren-9-one-->Spiro[1,3-dithiolane-2,9'-[9H]fluorene],2',7'-dibroMo--->Ethanol
Tag:2,7-DibroMo-9,9-difluoro-9H-fluorene(1229603-71-7) Related Product Information
Ledipasvir ledipasvir interMediate tert-Butyl 6-(5-(7-bromo-9,9-difluoro-9H-fluoren-2-yl) 2,7-DibroMo-9,9-difluoro-9H-fluorene (S)-2-((Methoxycarbonyl)aMino)-3-Methylbutanoic acid 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 3-(6-broMo-1H-benziMidazol-2-yl)-, 1,1-diMethylethyl ester,(1R,3S,4S)- (S)-5-BOC-5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID 1-(7-broMo-9,9-difluoro-9H-fluoren-2-yl)-2-chloro-Ethanone ledipasvir interMediate (3S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid