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Chemical Structure| 122699-51-8 Chemical Structure| 122699-51-8

Structure of 122699-51-8

Chemical Structure| 122699-51-8

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Product Details of [ 122699-51-8 ]

CAS No. :122699-51-8
Formula : C10H16O2
M.W : 168.23
SMILES Code : O=C(C1CC(C1)=C)OC(C)(C)C
MDL No. :MFCD26402411

Safety of [ 122699-51-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335-H227
Precautionary Statements:P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501

Application In Synthesis of [ 122699-51-8 ]

* 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 [ 122699-51-8 ]

[ 122699-51-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 15760-36-8 ]
  • [ 122699-51-8 ]
YieldReaction ConditionsOperation in experiment
48% With dmap; In tetrahydrofuran; at 20℃; To a solution of 3-methylene-cyclobutanecarboxylic acid Intermediate A14 (13.0 g,116 mmol) in tetrahydrofuran (150 mL) was added di-t-butyldicarbonate (33.0 g, 151 mmol) and 4-dimethylaminepyridine (2.83 g, 23.2 mmol). After stirred at room temperature overnight, the mixture was diluted with ethyl acetate (200 mL), washed with water (50 mL), brine (50 mL), dried over Na2 SO4() and filtered. The filtrate was concentrated under reduced pressure to give a residue, which was purified by silica gelcolumn chromatography (100 % petroleum ether) to give the title compound (9.4 g, 48 %yield) as colorless oil. ‘H NIVIR (400 1VIHz, DMSO-d6) 4.79 - 4.77 (m, 2H), 3.07 -2.99 (m, 1H), 2.88 - 2.77 (m, 4H), 1.40 (s, 9H).
 

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