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Chemical Structure| 1214900-59-0 Chemical Structure| 1214900-59-0

Structure of 1214900-59-0

Chemical Structure| 1214900-59-0

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Product Details of [ 1214900-59-0 ]

CAS No. :1214900-59-0
Formula : C9H10BrFO
M.W : 233.08
SMILES Code : CCC(C1=CC=C(Br)C=C1F)O
MDL No. :MFCD19601830

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Application In Synthesis of [ 1214900-59-0 ]

* 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 [ 1214900-59-0 ]

[ 1214900-59-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1214900-59-0 ]
  • [ 259750-61-3 ]
YieldReaction ConditionsOperation in experiment
76% With dipyridinium dichromate; In N,N-dimethyl-formamide; at 20℃; for 12.0h; Intermediate 100 1-(4-bromo-2-fluorophenyl)propan-1-one To a solution of intermediate 99 (5.8 g, 24.89 mmoles) in DMF (30 ml), pyridinium dichromate (14.04 g, 37.33 mmoles) was added at room temperature. After 12 h, the reaction mixture was quenched with water, diluted with ethyl acetate and filtered through celite. The organic layer was washed with brine solution and dried over sodium sulphate and concentrated under reduced pressure to afford the title compound as colourless liquid (4.4 g, 76% yield). 1H-NMR (delta ppm, DMSO-d6, 400 MHz): delta 7.78 (t, J=8.1 Hz, 1H), 7.38 (m, 2H), 2.55 (m, 2H), 1.21 (t, J=7.1 Hz, 3H).
1.84 g With manganese(IV) oxide; In 1,4-dioxane; at 80℃; for 16.0h; To a solution of the compound [140-1] obtained in the process (1) (3.78 g) in 1,4-dioxane (50 mL) was added manganese dioxide (10.6 g) at room temperature, and then the reaction mixture was stirred at 80C for 16 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the titled compound (1.84 g) as a white solid. 1H-NMR (400 MHz, CDCl3) delta: 7.77 (1H, t, J = 8.2 Hz), 7.40-7.30 (2H, m), 3.02-2.94 (2H, m), 1.20 (3H, t, J = 7.2 Hz).
 

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