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Chemical Structure| 864498-49-7 Chemical Structure| 864498-49-7

Structure of 864498-49-7

Chemical Structure| 864498-49-7

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Product Details of [ 864498-49-7 ]

CAS No. :864498-49-7
Formula : C8H12O3
M.W : 156.18
SMILES Code : O=C(OC)C(C)C(C1CC1)=O
MDL No. :MFCD16077060

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Application In Synthesis of [ 864498-49-7 ]

* 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 [ 864498-49-7 ]

[ 864498-49-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32249-35-7 ]
  • [ 74-88-4 ]
  • [ 864498-49-7 ]
YieldReaction ConditionsOperation in experiment
91% To a mixture of methyl 3 -cyclopropyl-3 -oxopropanoate (15 g, 0.11 mol, 1.0 eq ) in THF (0.10 L) was added CS2CO3 (52 g, 0.16 mol, 1.5 eq). The mixture was stirred at 20 C for 0.5 hours and then was added CH3I (15 g, 0.11 mol, 6.6 mL, 1.0 eq) at 20 C under N2. The mixture was stirred at 40 C for 2.5 hours. The reaction mixture was filtered, and the filtrate cake was washed with EtOAc (150 mL><3). The combined organic phase was concentrated to give 1 (15 g, 91% yield) as a yellow oil. NMR (400 MHz, CD Cl 3 -i ) d ppm 3.75 - 3.73 (m, 3 H), 3.71 - 3.64 (m, 1 H), 2.05 (t, J= 7.6, 4.4 Hz, 1 H), 1.42 - 1.38 (m, 3 H), 1.12 - 1.01 (m, 2 H), 0.97 - 0.86 (m, 2 H).
To a slurry of NaH (0.563 g, 60% in mineral oil) in THF (20 mL) was cooled to 10 0 C, then <strong>[32249-35-7]methyl 3-cyclopropyl-3-oxopropanoate</strong> (2 g) was added in portions at room temperature over 30 min. Then Mel (0.88 mL) was added over 5 min at room temperature and stirred at room temperature overnight. The reaction was reverse quenched into a half saturated sodium bicarbonate solution (100 mL) and EtOAc (100 mL). The aqueous layer was separated and extracted once with 50 mL EtOAc. The combined organic layers were washed with water and brine, and concentrated to give the title compound, which wast aken on to next the step without further purification.
With sodium hydride; In tetrahydrofuran; mineral oil; at 10 - 25℃; for 0.583333h; Step 1: methyl 3-cyclopropyl-2-methyl-3-oxopropanoate A slurry of NaH (0.5 63 g, 60% in mineral oil) in THF (20 mL) was cooled to 10 C, then <strong>[32249-35-7]methyl 3-cyclopropyl-3-oxopropanoate</strong> (2 g) wasadded in portions at rt over 30 minutes. Then Mel (0.88 mL) was added over 5 minutes at rt and the reaction was stirred at rt overnight. The reaction was then reverse quenched into a half saturated sodium bicarbonate solution (100 mL) and EtOAc (100 mL). The aqueous layer was separated and extracted once with 50 mL EtOAc. The combined organic layers were washed with water and brine, and concentrated to give the title compound, which was used in the next step without furtherpurification.
A slurry of NaH (0.563 g, 60in mineral oil) in THF (20 mL) was cooled to 10 , and <strong>[32249-35-7]methyl 3-cyclopropyl-3-oxopropanoate</strong> (2 g) was added in portions at room temperature over 30 min. Then MeI (0.88 mL) was added over 5 min at room temperature and the reaction was stirred at room temperature overnight. The reaction was then reverse quenched into a half saturated sodium bicarbonate solution (100 mL) and EtOAc (100 mL) . The aqueous layer was separated and extracted once with 50 mL EtOAc. The organic layer was washed with water and brine, and then concentrated to give the title compound, which was used in the next the step without further purification.
A slurry of NaH (0.563 g, 60% in mineral oil) in THF (20 mL) was cooled to 10 C, then <strong>[32249-35-7]methyl 3-cyclopropyl-3-oxopropanoate</strong> (2 g) was added in portions at room temperature over 30 minutes. Then Mel (0.88 mL) was added over 5 minutes at room temperature and the reaction was stirred at room temperature overnight. The reaction was then reverse quenched into a half saturated sodium bicarbonate solution (100 mL) and EtOAc (100 mL). The aqueous layer was separated and extracted once with 50 mL EtOAc. The combined organic layers were washed with water and brine, and concentrated to give the title compound, which was used in the next step without further purification.

 

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