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Chemical Structure| 2305-05-7 Chemical Structure| 2305-05-7

Structure of 2305-05-7

Chemical Structure| 2305-05-7

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Product Details of [ 2305-05-7 ]

CAS No. :2305-05-7
Formula : C12H22O2
M.W : 198.30
SMILES Code : CCCCCCCCC1CCC(O1)=O
English Name :5-Octyldihydrofuran-2(3H)-one
MDL No. :MFCD00036499
InChI Key :WGPCZPLRVAWXPW-UHFFFAOYSA-N
Pubchem ID :16821

Safety of [ 2305-05-7 ]

Application In Synthesis of [ 2305-05-7 ]

* 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 [ 2305-05-7 ]

[ 2305-05-7 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 2305-05-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
93% With sodium hydroxide In methanol at 20℃; for 24h;
With sodium hydroxide In ethanol for 2h; Yield given;
With sodium hydroxide In water at 100℃; for 12h; Inert atmosphere; 34.1 Step 1 : To a solution of 5 -octyltetrahydrofuran -2-one (50 g, 252.14 mmol, 1 eq) in H2O(500 mL) was added NaOH (10.59 g, 264.75 mmol, 1.05 eq) under N2 atmosphere. The reaction mixture was stirred at 100 °C for 12 hr under N2 atmosphere. The reaction mixture was concentrated under reduced pressure to remove solvent. Compound 4-hydroxydodecanoyloxysodium (50 g, crude) was obtained as a white solid and it was used in next step directly.
With sodium hydroxide In water at 120℃; for 2h; Inert atmosphere; 24 Intermediate 24g: sodium 4-hydroxydodecanoate To a solution of 5-octyltetrahydrofuran-2-one (50 g, 1.0 equiv.) in H2O (0.5 M) was added NaOH (1.0 - 1.1 equiv.). The mixture was degassed, purged 3x with N2 and stirred at 20 °C for 12 h. The reaction mixture was concentrated to afford the crude product that was used directly in the next step without additional purification (83%).

  • 2
  • [ 872-05-9 ]
  • [ 73664-43-4 ]
  • [ 2305-05-7 ]
YieldReaction ConditionsOperation in experiment
65% With bis(tri-n-butyltin); ethyl iodide Irradiation;
  • 3
  • [ 74646-36-9 ]
  • [ 2305-05-7 ]
YieldReaction ConditionsOperation in experiment
61% With 1-hydroxy-pyrrolidine-2,5-dione; trifuran-2-yl-phosphane; tetrabutylammomium bromide In water; N,N-dimethyl-formamide at 95℃; for 24h;
  • 4
  • [ 2430-94-6 ]
  • [ 2305-05-7 ]
YieldReaction ConditionsOperation in experiment
66% With silver trifluoromethanesulfonate In chlorobenzene at 130℃; for 24h; Inert atmosphere; regioselective reaction;
  • 5
  • [ 2305-05-7 ]
  • [ 38146-95-1 ]
YieldReaction ConditionsOperation in experiment
100% With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 24h; Inert atmosphere;
89% With phenylsilane; potassium hydroxide In tetrahydrofuran for 4h; Schlenk technique; Inert atmosphere; Reflux; 3. General procedure for synthesis of products (2) General procedure: Isobenzofuran-1(3H)-one (0.4 mmol), KOH (0.4 mmol), PhSiH3 (1.2 mmol), dried THF (2 mL) were charged in a Schlenk tube(15 mL) under N2 atmosphere. The mixture was refluxed for 4 h. After cooling to rt, the reaction was quenched with EtOH(0.5-1 mL). Solvent was removed under reduced pressure and the crude residue was purified by column chromatography on silica gel with petroleum ether-ethyl acetate as the eluent to afford the desired product.
 

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