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Chemical Structure| 132180-14-4 Chemical Structure| 132180-14-4

Structure of 132180-14-4

Chemical Structure| 132180-14-4

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Product Details of [ 132180-14-4 ]

CAS No. :132180-14-4
Formula : C9H16O4
M.W : 188.22
SMILES Code : O=C(OC(C)(C)C)C(C)C(OC)=O
InChI Key :JDQGMPGKDBIWOI-UHFFFAOYSA-N
Pubchem ID :25198323

Safety of [ 132180-14-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 132180-14-4 ]

* 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 [ 132180-14-4 ]

[ 132180-14-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 42726-73-8 ]
  • [ 74-88-4 ]
  • [ 132180-14-4 ]
YieldReaction ConditionsOperation in experiment
77% A 100 mL round-bottom flask equipped with a stirring bar was charged with compound 7 (1920 mg, 11.0 mmol) and DMF (25 mL). To the solution, sodium hydride (60percent oil suspension, 446 mg, 11.0 mmol) was added. The reaction was allowed to stir at 0 °C for 30 h. To the mixture, methyl iodide (670 muL, 11.0 mmol) was added at 0 °C and the mixture was stirred at room temperature for 18 h. To the reaction mixture, H2O was added, and the mixture was extracted with CH2Cl2 (3x), dried over MgSO4, and concentrated in vacuo. The remaining residue was purified by silica gel column chromatography (hexanes/AcOEt = 90:10) to afford the desired product 3 (1597 mg, 77percent) as a colorless oil. 1H NMR (400 MHz, CDCl3) delta 3.73 (s, 3H), 3.35 (q, J = 7.3 Hz, 1H), 1.46 (s, 9H), 1.38 (d, J = 7.3 Hz, 3H); 13C NMR (100 MHz, CDCl3) delta 170.9, 169.2, 81.6, 52.2, 47.0, 27.8, 13.5.
9.91 Gram (95percent, 56.9 mmol) of <strong>[42726-73-8]tert-butyl methyl malonate</strong> was dissolved in 120 mL of tetrahydrofuran (THF), and the resulting solution was added dropwise to a suspension containing 2.28 g (60 wtpercent, 56.9 mmol) of sodium hydride (NaH) and 120 mL of THF at 0°C over 0.5 hours, followed by stirring for 0.5 hours. Thereafter, a solution containing 8.08 g (56.9 mmol) of methyl iodide (Mel) and 20 mL of THF was added dropwise over 0.5 hours, and the resulting mixture was stirred at 0°C for 0.5 hours and further stirred at 25°C for 5 hours. After adding 200 mL of ethyl acetate, the organic layer was washed, in order, twice with saturated brine and twice with water, and dried over sodium sulfate, and the solvent was concentrated to obtain 13.0 g of 1-tert-butyl 3-methyl 2-methylmalonate as a colorless transparent oil. Subsequently, 45.9 g of an aqueous formalin solution was added to 13.0 g of the oil, and resulting mixture was cooled to 0°C. Furthermore, 7.81 g of potassium carbonate was added, and the mixture was stirred at 0°C for 1 hour and further stirred at 25°C for 3 hours. After adding 200 mL of ethyl acetate, the organic layer was washed, in order, three times with an aqueous saturated sodium hydrogensulfite solution and twice with water, and dried over sodium sulfate. The solvent was concentrated, and the residue was dissolved in 50 mL of pyridine. The resulting solution was cooled to 0°C, and 21.7 g of p-toluenesulfonyl chloride was added thereto. The obtained mixture was stirred at 0°C for 2 hours and then stirred at 60°C for 4 hours. After adding 200 mL of ethyl acetate, the organic layer was washed, in order, three times with an aqueous saturated ammonium chloride solution and twice with water, and dried over sodium sulfate. The residue was purified by column chromatography (SiO2, hexane/ethyl acetate=4/1) to obtain 15.8 g of the objective Compound (I-31) as a colorless transparent oil. 1H-NMR (400 MHz, CDCl3) delta 1.40 (s, 9H), 1.43 (s, 3H), 2.45 (s, 3H), 3.67 (s, 3H), 4.30 (s, 2H), 7.36 (d, 2H), 7.77 (d, 2H).
  • 2
  • [ 42726-73-8 ]
  • methyl halide [ No CAS ]
  • [ 132180-14-4 ]
YieldReaction ConditionsOperation in experiment
General procedure: alpha-Monosubstituted malonic diester 1 was synthesized according to the reported procedure as follows.3 tert-Butyl methyl malonate was purchased from Kanto Chemical, and used without further purification. The physical properties and spectral data of the new compounds, 2-(2-methylbenzyl)malonate 1g, 2-prenylmalonate 1l, and 2-(2-benzyloxyethyl)malonate 1o, are listed below. A 100 mL round-bottom flask equipped with a stirring bar was charged with <strong>[42726-73-8]tert-butyl methyl malonate</strong> (846 muL, 5.0 mmol) and DMF (10 mL). To the solution, sodium hydride (60percent oil suspension, 200 mg, 5.0 mmol) was added. The reaction was allowed to stir at 0 °C for 30 min. To the mixture, corresponding alkyl halide (5.0 mmol) was added at 0 °C and the mixture was stirred at room temperature for 24 h. To the reaction mixture, H2O was added, and the mixture was extracted with CH2Cl2 (3 * 20 mL), dried over MgSO4, and concentrated in vacuo. The remaining residue was purified by silica gel column chromatography (hexane/ethyl acetate) to afford the desired product 1.
 

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