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Chemical Structure| 7515-27-7 Chemical Structure| 7515-27-7

Structure of 7515-27-7

Chemical Structure| 7515-27-7

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Product Details of [ 7515-27-7 ]

CAS No. :7515-27-7
Formula : C10H8O2
M.W : 160.17
SMILES Code : O=C(O)C#CC1=CC=CC=C1C
MDL No. :MFCD14707283

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Application In Synthesis of [ 7515-27-7 ]

* 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 [ 7515-27-7 ]

[ 7515-27-7 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 615-37-2 ]
  • [ 471-25-0 ]
  • [ 7515-27-7 ]
YieldReaction ConditionsOperation in experiment
56% With bis-triphenylphosphine-palladium(II) chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,4-di(diphenylphosphino)-butane; In dimethyl sulfoxide; at 50℃; for 5h;Sealed flask; General procedure: Method A; Pd(PPh3)2Cl2 (35.1 mg, 0.05 mmol), 1,4-bis(diphenylphosphino)butane (42.6 mg, 0.1 mmol), aryl halides (2.0 mmol), and DBU (1.52 g, 10.0 mmol) were combined with DMSO (4.0 mL), in a small round-bottomed flask. Propiolic acid (1a) (140.0 mg, 2.0 mmol) was added, and the flask was sealed with a septum. The resulting mixture was placed in an oil bath at 50 C for 5 h. The reaction was poured into Ethyl acetate and extracted with water saturated by NaHCO3. The aqueous layer was acidified to pH 2.0 by cold 1 N HCl(aq) and extracted with CH2Cl2. The organic layer dried over MgSO4, and filtered. The solvent was removed under vacuum, and the resulting crude product was purified by flash chromatography on silica gel to give 3a (208.6 mg, 96% yield). The spectroscopic data of 3a-j are as follows.
With tetrakis(triphenylphosphine) palladium(0); 1,8-diazabicyclo[5.4.0]undec-7-ene; In dimethyl sulfoxide; at 20℃; for 12h; In a reaction vessel, o-methyl iodobenzene (10.0 mmol), DBU (3.66 g, 24 mmol, 2.4 equiv), Pd(PPh4)3 (288 mg, 0.26 mmol, 2.5 mol %)Dissolve in 12 ml of DMSO to form solution a, then dissolve the propiolic acid (840 mg, 12 mmol, 1.2 equiv) in 12 ml of DMSO.Solution b was formed, and finally solution b was slowly added dropwise to solution a and stirred at room temperature for 12 hours.After the reaction was completed, 25 ml of ethyl acetate was added to the reaction solution, and the mixture was extracted with a saturated sodium bicarbonate solution.The collected aqueous layer was adjusted to pH 2.0 with 1 mol/L hydrochloric acid, and finally the organic layer was extracted with dichloromethane extraction.The organic phase was separated and dried over anhydrous sodium sulfate. After drying, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was isolated by column chromatography to obtain o-methylphenylpropiolic acid compound.
With tetrakis(triphenylphosphine) palladium(0); 1,8-diazabicyclo[5.4.0]undec-7-ene; In dimethyl sulfoxide; at 35℃; for 10h;Inert atmosphere; To a 100 mL of round-bottom flask were added Pd(PPh3)4 (577.8 mg, 5 mol%), aryl iodide (10.0 mmol, 1.0 equiv), DBU (3.040 g, 20 mmol, 2.0 equiv) and DMSO (15 mL). Then the solution of propiolic acid (771 mg, 11 mmol, 1.1 equiv) in DMSO (5 mL) was added dropwise. The round-bottom flask was put into a preheated oil bath (35 C). After stirring for 10 h, the reaction mixture was cooled to room temperature. The reaction mixture was diluted with EtOAc, and extracted with saturated aqueous NaHCO3 solution. The aqueous layer was separated, acidified to pH 2.0 by cold HCl (1N), and extracted with CH2Cl2. The combined organic layers were dried with Na2SO4, filtered, and the solvent was removed under reduced pressure. The resulting crude product was purified by flash chromatography on silica gel (PE/EA = 2:1 with HOAc (1%, v/v)) to give 1b-1q.
 

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