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Chemical Structure| 4415-76-3 Chemical Structure| 4415-76-3

Structure of 4415-76-3

Chemical Structure| 4415-76-3

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Product Details of [ 4415-76-3 ]

CAS No. :4415-76-3
Formula : C6H10O
M.W : 98.14
SMILES Code : OCC=C1CCC1
MDL No. :MFCD24369225

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Application In Synthesis of [ 4415-76-3 ]

* 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 [ 4415-76-3 ]

[ 4415-76-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27741-65-7 ]
  • [ 4415-76-3 ]
YieldReaction ConditionsOperation in experiment
84% With diisobutylaluminium hydride; In dichloromethane; toluene; at -78℃;Inert atmosphere;Product distribution / selectivity; In 40 mL of dry DCM, <strong>[27741-65-7]ethyl 2-cyclobutylideneacetate</strong> (0.85 g, 6.07 mmol) was dissolved and mixture allowed to cool to -78 C. under nitrogen atmosphere. To this solution DIBAL-H (1M in toluene) (1.72 g, 12.1 mL, 12.1 mmol) was added dropwise. Reaction was monitored by TLC (20% ethyl acetate in n-hexane), when starting material (Rf=0.28) was completely consumed reaction mixture was quenched with MeOH/H2O (1:1). DCM layer was separated and dried over sodium sulfate. DCM was removed under reduced pressure. Crude product was purified by column chromatography (silica gel 60-120 mesh, 0-20% ethyl acetate in n-hexane) afforded pure product as colorless oil.Yield: 0.5 g (84%)1H NMR (400 MHz, CDCl3): delta 1.61 (br, 1H), 1.91-2.05 (m, 2H), 2.65-2.74 (m, 4H), 4.02 (d, J=7.2 Hz, 2H), 5.30-5.36 (m, 1H).
84% With diisobutylaluminium hydride; In dichloromethane; toluene; at -78℃;Inert atmosphere; In 40 mL of dry DCM <strong>[27741-65-7]ethyl 2-cyclobutylideneacetate</strong> (0.85 g, 6.07 mmol) was allowed to cool to -78 C. under nitrogen atmosphere. To this solution DIBAL-H (1M in toluene) (1.72 g, 12.1 mL, 12.1 mmol) was added dropwise. Reaction was monitored by TLC. When the starting material was consumed completely the reaction mixture was quenched with MeOH/H2O (1:1) (Rf=0.28, 20% ethyl acetate/n-hexane). DCM layer was separated and dried over sodium sulphate. DCM was removed under reduced pressure. Crude product was purified by column chromatography (silica gel 60-120 mesh, 0-20% ethyl acetate and n-hexane as eluent) afforded colorless oil. [0545] Yield: 0.5 g (84%) [0546] 1H NMR (400 MHz, CDCl3): delta 1.61 (br, 1H), 1.91-2.05 (m, 2H), 2.65-2.74 (m, 4H), 4.02 (d, J=7.2 Hz, 2H), 5.30-5.36 (m, 1H).
 

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