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Chemical Structure| 141979-56-8 Chemical Structure| 141979-56-8

Structure of 141979-56-8

Chemical Structure| 141979-56-8

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Product Details of [ 141979-56-8 ]

CAS No. :141979-56-8
Formula : C12H18O7
M.W : 274.27
SMILES Code : CC(=O)OC[C@H]1OC(OC(C)=O)[C@@H]2OC(C)(C)O[C@H]12
MDL No. :MFCD09750744

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Application In Synthesis of [ 141979-56-8 ]

* 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 [ 141979-56-8 ]

[ 141979-56-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18163-47-8 ]
  • [ 141979-56-8 ]
  • 1-trimethylsilylethynyl-5-O-acetyl-2,3-O-isopropylidene-β-D-ribofuranose [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% A suspension of In(0) (0.75 g, 6.56 mmol) in anhyd 1,2-dichloroethane (10 mL) under argon was stirred for 20 min at r.t. 1-Iodo-2-trimethylsilylacetylene (1.2 g, 5.47 mmol) and the ribofuranoside 2 (0.75 g, 2.73 mmol) were added to the reaction tube, which was sealed, then evacuated, and backfilled with argon (this process was repeated a total of 3 times). The reaction mixture was stirred for 6 h at 90 C. The mixture was filtered over Celite and evaporated. The crude residue was taken in anhyd acetone (4 mL) and treated with p-TsOH·H2O (16 mg, 3 mol%). After stirring at r.t. for 5 h, the mixture was neutralized with NaHCO3, filtered through Celite, and concentrated under reduced pressure. The crude residue obtained was purified by flash column chromatography on silica gel (cyclohexane/EtOAc3:1) to give 9 as a yellow oil; yield: 431 mg (58% from 2); [alpha]D25 +22.0(c 1.5, CHCl3). 1H NMR (400 MHz, CDCl3): delta = 4.81 (dd, J = 6.4, 2.2 Hz, 1 H), 4.66-4.69 (m, 2 H), 4.09-4.34 (m, 3 H), 2.09 (s, 3 H), 1.50 (s, 3 H), 1.33 (s, 3 H), 0.15 (s, 9 H). 13C NMR (100 MHz, CDCl3): delta = 170.69, 114.06, 102.74, 92.77, 86.54, 83.71, 82.98, 75.18, 63.94, 26.95, 25.42, 20.97, 20.26. HRMS: m/z [M + H]+ calcd for C15H25O5Si: 313.1466; found: 313.1471.
40% With indium; In 1,2-dichloro-ethane; for 4h;Reflux; Inert atmosphere; A suspension of indium powder (10.0 g, 88 mmol) in DCE (50 mL) was stirred at room temperature for 20 min under nitrogen atmosphere. A solution of Intermediate 1G (10.0 g, 36.5 mmol) and (iodoethynyl)trimethylsilane (11 mL, 72.9 mmol) in DCE (10 mL) was added to the reaction flask via syringe, followed by 2 x 5 mL rinses with DCE (10 mL). The reaction flask was outfitted with a reflux condenser and the entire setup was evacuated and backfllled with nitrogen 3 times. The reaction was then stirred at reflux for 4 hours under nitrogen atmosphere. The crude reaction mixture was filtered through a pad of Celite (rinsed copiously with acetone) and the filtrate was concentrated in vacuo to afford a tarry dark oil. The crude product was purified by flash chromatography (SiC , 750 g column, 0% to 30% EtOAc/hexanes, 44 min gradient, 300 mL/min) to afford (0830) Intermediate IH (4.56 g, 14.6 mmol, 40% yield). NMR (500 MHz, CHLOROFORM- d) delta 4.82 (dd, J=6.2, 2.4 Hz, IH), 4.70 - 4.66 (m, 2H), 4.34 - 4.19 (m, 3H), 2.10 (s, 3H), 1.52 (s, 3H), 1.35 (s, 3H), 0.17 (s, 9H).
 

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