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Chemical Structure| 83852-61-3 Chemical Structure| 83852-61-3

Structure of 83852-61-3

Chemical Structure| 83852-61-3

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Product Details of [ 83852-61-3 ]

CAS No. :83852-61-3
Formula : C12H18O4
M.W : 226.27
SMILES Code : C/C(CC/C=C(C)/C(O)=O)=C\COC(C)=O

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Application In Synthesis of [ 83852-61-3 ]

* 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 [ 83852-61-3 ]

[ 83852-61-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 37905-02-5 ]
  • [ 83852-61-3 ]
YieldReaction ConditionsOperation in experiment
100% Example 9 Preparation of 8-Acetoxy-2,6-dimethyl-octa-2,6-dienoic acid (232a) To a solution of aldehyde 230a (19.5 g, 92.7 mmol) in 300 mL of tert-butyl alcohol was added 2-methyl-2-butene (98.0 mL, 925 mmol). To this was added a solution of sodium dihydrogen phosphate (44.5 g, 371 mmol) in 300 mL of water. Sodium chlorite (33.6 g, 371 mmol) was added in several portions. The resulting mixture was rapidly stirred overnight at room temperature. Ethyl acetate was added and the aqueous layer was acidified to pH 3 by addition of 1 M HCl. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3*200 mL). The combined organic extracts were washed with brine, dried over MgSO4, and reduced to dryness in vacuo. The crude product (27.4 g, 121 mmol, >100% yield) was used in the next step without further purification: 1H NMR (500 MHz, CDCl3) δ: 6.84 (t of q, J=7.25 Hz, J=1.50 Hz, 1H, =CH), 5.34 (t of q, J=7.00 Hz, J=1.50 Hz, 1H, =CH), 4.56 (d, J=7.00 Hz, 2H, -CH2O-), 2.31 (q, J=7.50 Hz, 2H, -CH2-), 2.15 (t, J=7.50 Hz, 2H, -CH2-), 2.03 (s, 3H, -CH3), 1.81 (s, 3H, -CH3), 1.70 (s, 3H, -CH3). LC/MS (ESI): m/z 249 [M+Na]+.
100% To a solution of aldehyde 230a (19.5 g, 92.7 mmol) in 300 mL of tert-bxxtyl alcohol was added 2-methyl-2- butene (98.0 mL, 925 mmol). To this was added a solution of sodium dihydrogen phosphate (44.5 g, 371 mmol) in 300 mL of water. Sodium chlorite (33.6 g, 371 mmol) was added in several portions. The resulting mixture was rapidly stirred overnight at room temperature. Ethyl acetate was added and the aqueous layer was acidified to pH 3 by addition of 1 MHCl. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3 x 200 mL). The combined organic extracts were washed with brine, dried over MgSO4, and reduced to dryness in vacuo. The crude product (27.4 g, 121 mmol, > 100 % yield) was used in the next step without further purification: 1H NMR (500 MHz, CDCl3) δ: 6.84(t of q, J= 7.25 Hz, J= 1.50 Hz, IH, =CH), 5.34 (t of q, J= 7.00 Hz, J= 1.50 Hz, IH, =CH), 4.56 (d, J= 7.00 Hz, 2H, -CH2O-), 2.31 (q, J = 7.50 Hz, 2H5 -CH2-), 2.15 (t, J= 7.50 Hz, 2H, -CH2- ), 2.03 (s, 3H, -CH3), 1.81 (s, 3H, -CH3), 1.70 (s, 3H, -CH3). LC/MS (ESI): m/∑2A9 [M+Naf.
 

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