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Chemical Structure| 2610-96-0 Chemical Structure| 2610-96-0

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Chemical Structure| 2610-96-0

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Product Details of [ 2610-96-0 ]

CAS No. :2610-96-0
Formula : C7H12O2
M.W : 128.17
SMILES Code : O=C1OC(C)(C)CC1C
MDL No. :MFCD22055952

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Application In Synthesis of [ 2610-96-0 ]

* 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 [ 2610-96-0 ]

[ 2610-96-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3123-97-5 ]
  • [ 74-88-4 ]
  • [ 2610-96-0 ]
YieldReaction ConditionsOperation in experiment
3.2 g 5,5-Dimethyldihydrofuran-2(3H)-one (4.7 g, 41.2 mmol) was dissolved in THF (94 mL) and the mixture was cooled to -78 C. under an atmosphere of argon. A solution of lithium diisopropylamide, 2.0 M solution in THF (22.6 mL, 45.2 mmol) was added dropwise over 10 min. The reaction was stirred at -78 C. for 2 h, and then neat MeI (2.6 mL, 41.6 mmol) was added to the reaction over 5 min. The reaction was stirred at -78 C. for 45 min, and then the mixture was allowed to warm to room temperature and stirred for 16 h. The reaction was quenched with saturated NH4Cl (25 mL) and the mixture concentrated to remove THF. The aqueous residue was diluted with H2O to dissolve solid and then extracted with ethyl acetate (3×40 mL). The combined organic layer was concentrated under vacuum, and the residue was purified by column chromatography on silica gel using EtOAc/hexanes (0:1 to 2:3) as eluent to provide a liquid which solidified on standing. This solid was purified further via Kugelrohr distillation to give the product (74a) (3.2 g) as an oil. 1H NMR (300 MHz, CDCl3): delta 2.78-2.87 (m, 1H), 2.33 (dd, J=9.3, 12.3 Hz, 1H), 1.71 (t, J=12.3 Hz, 1H), 1.45 (s, 3H), 1.38 (s, 3H), 1.29 (d, J=6.9 Hz, 3H).
3.2 g 5,5-Dimethyldihydrofuran-2(3H)-one (4.7 g, 41.2 mmol) was dissolved in 48 THF (94 mL) and the mixture was cooled to ?78° C. under an atmosphere of argon. A solution of 463 lithium diisopropylamide, 2.0 M solution in THF (22.6 mL, 45.2 mmol) was added dropwise over 10 min. The reaction was stirred at ?78° C. for 2 h, and then neat 129 MeI (2.6 mL, 41.6 mmol) was added to the reaction over 5 min. The reaction was stirred at ?78° C. for 45 min, and then the mixture was allowed to warm to room temperature and stirred for 16 h. The reaction was quenched with saturated 132 NH4Cl (25 mL) and the mixture concentrated to remove THF. The aqueous residue was diluted with H2O to dissolve solid and then extracted with ethyl acetate (3×40 mL). The combined organic layer was concentrated under vacuum, and the residue was purified by column chromatography on silica gel using 21 EtOAc/hexanes (0:1 to 2:3) as eluent to provide a liquid which solidified on standing. This solid was purified further via Kugelrohr distillation to give the 653 product (98a) (3.2 g) as an oil. 1H-NMR (300 MHz, CDCl3): delta 2.78-2.87 (m, 1H), 2.33 (dd, J=9.3, 12.3 Hz, 1H), 1.71 (t, J=12.3 Hz, 1H), 1.45 (s, 3H), 1.38 (s, 3H), 1.29 (d, J=6.9 Hz, 3H).
 

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