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Chemical Structure| 749928-88-9 Chemical Structure| 749928-88-9

Structure of 749928-88-9

Chemical Structure| 749928-88-9

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Product Details of [ 749928-88-9 ]

CAS No. :749928-88-9
Formula : C10H7BrFN
M.W : 240.07
SMILES Code : N#CC1(C2=CC=C(Br)C=C2F)CC1
MDL No. :MFCD18909162

Safety of [ 749928-88-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P264-P270-P280-P301+P312+P330-P305+P351+P338-P337+P313-P501

Application In Synthesis of [ 749928-88-9 ]

* 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 [ 749928-88-9 ]

[ 749928-88-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 749928-88-9 ]
  • [ 872422-15-6 ]
YieldReaction ConditionsOperation in experiment
100% With water; potassium hydroxide; In ethanol; for 7h;Reflux; A solution of the compound (24.6 g, 102 mmol) obtained in Example 14-2) and potassium hydroxide (46 g, 820 mmol) in ethanol (200 ml) and water (40 ml) was heated to reflux for 7 h. The reaction mixture was cooled to room temperature, and then 5 N hydrochloric acid was added until the reaction mixture was rendered acidic. The deposited solid was collected by filtration, washed with water, and then dried to obtain the title compound (28.7 g, quant.) as a colorless solid. 1H-NMR (400 Hz, CDCl3) delta: 1.23 (2H, m), 1.72 (2H, m), 7.10-7.15 (1H, m), 7.22-7.25 (2H, m)
10.87 g With water; lithium hydroxide; at 100℃; In a 1 L round-bottomed flask, l-(4-bromo-2-fluorophenyl)cyclopropanecarbonitrile (1 1.2 g, 46.7 mmol) and LiOH (58 g, 1.38 mol) were combined with water (230 mL) to give a yellow suspension. The mixture was heated in an oil bath at 100 C overnight. The mixture was diluted to 1 L with water and ice and extracted with ethyl ether (3 x 300 mL). There was some white insoluble material between phases that was not included in aqueous layer. The aqueous layer was acidified with concentrated HC1 (ca. 1 10 mL) slowly with addition of ice. A very fine precipitate formed and the milky solution was not filtered but extracted with DCM (4 x 250 ml). The organic layers were combined, dried over MgS04, filtered, and concentrated yielding l-(4-bromo-2-fluorophenyl)cyclopropanecarboxylic acid (10.87 g, 89.9% yield) as a yellow solid. LC/MS calcd. for Ci0H8BrFO2 (m/e) 258/260, obsd. 259/261 (M+H, ES+).
 

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