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[ CAS No. 77758-51-1 ] {[proInfo.proName]}

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Chemical Structure| 77758-51-1
Chemical Structure| 77758-51-1
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Product Details of [ 77758-51-1 ]

CAS No. :77758-51-1 MDL No. :MFCD00671366
Formula : C7H10O2 Boiling Point : -
Linear Structure Formula :CH3OCOC3H6CCH InChI Key :LZULAZTXJLWELL-UHFFFAOYSA-N
M.W : 126.15 Pubchem ID :534077
Synonyms :

Safety of [ 77758-51-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P337+P313 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 77758-51-1 ]

* 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 [ 77758-51-1 ]

[ 77758-51-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 77758-51-1 ]
  • [ 75676-72-1 ]
  • [ 414861-73-7 ]
  • 2
  • [ 130723-13-6 ]
  • [ 77758-51-1 ]
  • [ 864755-92-0 ]
YieldReaction ConditionsOperation in experiment
81% With triethylamine;bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; at 20 - 80℃; for 24h; 6-(3-Fluoro-5-trifluoromethylphenyl)-hex-5-ynoic Acid Methyl Ester (41). Pd(PPh3)2Cl2 (236 mg, 0.336 mmol) was added to a mixture of bromide 38 (1.677 g, 6.70 mmol) and methyl 5-hexynoate (1.025 g, 8.12 mmol) in triethylamine (5.0 mL) at room temperature. Cu(I)I (136 mg, 0.714 mmol) was added. The resulting mixture was stirred at room temperature for 1.5 h and at 80 C. for 22.5 h. The reaction mixture was cooled to room temperature, filtered through a short column of silica gel (5 g), and the column was washed with ethyl acetate. The organic solution was concentrated. The residue was purified by column chromatography on silica gel (40 g), eluting with EtOAc-hexanes (2%) to afford the product 41 (1.564 g) as a white solid in 81% yield: mp 44-45 C. IR (KBr) 3084, 2955, 2848, 2238, 1740, 1619, 1599, 1467, 1439, 1363, 1253, 1240, 1224, 1171, 1133, 1093, 1046, 995, 973, 924, 911, 875, 695 cm-1; 1H NMR (300 MHz, CDCl3) delta 7.40 (s, 1H), 7.21 (m, 2H), 3.66 (s, 3H), 2.47 (t, J=7.2 Hz, 4H), 1.90 (m, 2H); 13C NMR (75 MHz, CDCl3) delta 173.3, 163.7, 160.4, 132.8, 132.3, 126.8, 126.7, 124.7, 124.3, 121.8, 121.5, 112.3, 111.9, 79.1, 51.6, 32.7, 23.5, 18.7; ESIMS m/z (rel intensity) 288.96 (MH+, 51). Anal. (C14H12F4O2) C, H, F.
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