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Chemical Structure| 141940-30-9 Chemical Structure| 141940-30-9

Structure of 141940-30-9

Chemical Structure| 141940-30-9

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Product Details of [ 141940-30-9 ]

CAS No. :141940-30-9
Formula : C12H14FNO4
M.W : 255.24
SMILES Code : O=C(O)C1=CC=CC(F)=C1NC(OC(C)(C)C)=O

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Application In Synthesis of [ 141940-30-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 141940-30-9 ]

[ 141940-30-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 124-38-9 ]
  • [ 98968-72-0 ]
  • [ 141940-30-9 ]
  • 2
  • [ 98968-72-0 ]
  • [ 141940-30-9 ]
YieldReaction ConditionsOperation in experiment
37% A solution of te/t-butyllithium in pentane (1.7M, 34ml, 58mmol) was added with caution to a solution of (2-fluoro-phenyl)-carbamic acid tert-butyl ester whilst cooling to less than -50C. The mixture was maintained at this tempera­ture, stirred for 3h then poured onto a slurry of THF and dry ice. The mixture was allowed to warm to room temperature, diluted with water and evaporated in vacuo. The residue was taken up in water and washed with diethyl ether. A solution of 0.3M potassium hydrogen sulphate was added until pH6 and ex­tracted with chloroform. The chloroform extracts were combined, washed with brine, dried and reduced to give a white solid; yield 2.7g, 37%.
With carbon dioxide; tert.-butyl lithium; In tetrahydrofuran; pentane; 2-(tert-Butoxycarbonylamino)-3-fluoro-benzoic acid To a solution of <strong>[98968-72-0]tert-butyl 2-fluorophenylcarbamate</strong> (44.0 g, 208 mmol) in tetrahydrofuran (660 mL) at -78 C. was added tert-butyllithium in pentane (1.7 M, 306 mL, 2.5 equivx) dropwise. After addition was complete, the reaction was stirred at -78 C. for 30 min. The solution was allowed to gradually reach -20 C. before being recooled to -78 C. and transferred via canula to a slurry of carbon dioxide (excess) and tetrahydrofuran (500 mL). The solution was allowed to slowly warm to room temperature. The reaction mixture was concentrated to remove most of the tetrahydrofuran, and poured into a sep funnel containing water and diethyl ether. The layers were separated, and the aqueous extracted with diethyl ether twice more. The ethereals were discarded. The aqueous was acidified with 5% citric acid, extracted with diethyl ether (3*). The ethereal was dried over magnesium sulfate, and concentrated to give a light yellow solid which was recrystallized from hot toluene to give 37.1 g (70%) as a faint yellow solid. 1H-NMR (CDCl3, 500 MHz) δ 1.50 (s, 9H), 6.25 (bs, 1H), 7.18 (ddd, J=7.9, 7.9, 4.9, 1H), 7.33 (dd, J=9.5, 9.2, 1H), 7.79 (d, J=7.9, 1H), 7.94 (s, 1H). Mass spec.: 278.21 (MNa)+.
 

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