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Chemical Structure| 28049-63-0 Chemical Structure| 28049-63-0

Structure of 28049-63-0

Chemical Structure| 28049-63-0

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Product Details of [ 28049-63-0 ]

CAS No. :28049-63-0
Formula : C11H10FN
M.W : 175.20
SMILES Code : N#CC1(C2=CC=CC=C2F)CCC1
MDL No. :MFCD11036671

Safety of [ 28049-63-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 28049-63-0 ]

* 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 [ 28049-63-0 ]

[ 28049-63-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 326-62-5 ]
  • [ 109-64-8 ]
  • [ 28049-63-0 ]
YieldReaction ConditionsOperation in experiment
53% With sodium hydride; In diethyl ether; dimethyl sulfoxide; at 20 - 30℃; Example 1Al-(2-fluorophenyl)cyclobutanecarbonitrileSodium hydride (0.317 g, 13.2 mmol) was slowly added to DMSO (40 mL) at 0 C, and the mixture was warmed to ambient temperature. After stirring for 10 minutes, a solution of 2-<strong>[326-62-5](2-fluorophenyl)acetonitrile</strong> (0.702 g, 6.0 mmol) and 1, 3-dibromopropane (1.206 g, 6.0 mmol) in diethyl ether (20 mL) was added over 30 min at < 30 C. Additional 10 mL ofDMSO was added to ease the stirring. The mixture was stirred overnight at room temperature and then diluted with 25 mL of ether and 15 mL of water. The organic layer was separated and washed with water and brine. After drying (Na2S04), filtering, and concentrating, the residue was purified by column chromatography on silica gel (petroleum ether: EtOAc=10:l) to give Example 1 A (0.5 g, 3.18 mmol, 53 % yield). LC-MS: m/z 176 (M+H).
53% With sodium hydride; In diethyl ether; dimethyl sulfoxide; mineral oil; at 20 - 30℃; Example 1A 1-(2-fluorophenyl)cyclobutanecarbonitrile Sodium hydride (0.317 g, 13.2 mmol) was slowly added to DMSO (40 mL) at 0 C., and the mixture was warmed to ambient temperature. After stirring for 10 minutes, a solution of 2-<strong>[326-62-5](2-fluorophenyl)acetonitrile</strong> (0.702 g, 6.0 mmol) and 1,3-dibromopropane (1.206 g, 6.0 mmol) in diethyl ether (20 mL) was added over 30 min at <30 C. Additional 10 mL of DMSO was added to ease the stirring. The mixture was stirred overnight at room temperature and then diluted with 25 mL of ether and 15 mL of water. The organic layer was separated and washed with water and brine. After drying (Na2SO4), filtering, and concentrating, the residue was purified by column chromatography on silica gel (petroleum ether: EtOAc=10:1) to give Example 1A (0.5 g, 3.18 mmol, 53% yield). LC-MS: m/z 176 (M+H).
51.4% With sodium hydride; In N,N-dimethyl-formamide; at 0 - 50℃; for 17h; 2-<strong>[326-62-5](2-fluorophenyl)acetonitrile</strong> (3.000 g, 22.199 mmol) and sodium hydride (60.00%, 1.953 g, 48.838 mmol) in N,N-dimethylformamide (150 mL) at 0 C to this mixture 1,3-dibromopropane (2.253 mL, 22.199 mmol) was added and stirred at 50 C for 17 hours, the temperature was lowered to room temperature, saturated sodium bicarbonate aqueous solution (10 mL) was added to the reaction mixture at 0 C, and the reaction was terminated by stirring for 10 minutes. The solvent was removed from the reaction mixture under reduced pressure, the obtained concentrate was poured into water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, and water was removed with anhydrous magnesium sulfate, followed by filtration and concentration under reduced pressure. The concentrate was purified by column chromatography (SiO2, 40 g cartridge; ethyl acetate/hexane = 0% to 10%) and concentrated to give the title compound (2.000 g, 51.4%) as a colorless oil.
With potassium hydroxide; In diethyl ether; dimethyl sulfoxide; at 20℃; for 1h; Potassium hydroxide (1.78 g) was dissolved in dimethyl sulfoxide (5.8 [ML)] [1]. (2-Fluorophenyl) acetonitrile (0.97 g, 7.2 mmol) and 1,3-dibromopropane (0.95 mL, 9.3 mmol) were dissolved in ethyl ether (2 [ML),] and this mixture was added dropwise to the potassium hydroxide solution while vigorously stirring at room temperature. After stirring at room temperature for one h, the reaction was quenched by adding ice-cold water (3.8 mL). The mixture was filtered through a pad of celite which was washed with ether (20 [ML).] The filtrate was added to a separatory funnel, and the aqueous layer was extracted with ether (3 x 10 [ML).] The organic layers were combined, dried over magnesium sulfate, filtered, and concentrated to give a light yellow oil (1.0 g). Pure [1- (2-FLUOROPHENYL) CYCLOBUTANECARBONITRILE] (0.45 g) was obtained after silica gel chromatography.

 

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