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Chemical Structure| 23709-41-3 Chemical Structure| 23709-41-3

Structure of 23709-41-3

Chemical Structure| 23709-41-3

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Product Details of [ 23709-41-3 ]

CAS No. :23709-41-3
Formula : C9H14O5
M.W : 202.20
SMILES Code : O=C1O[C@H](CO)[C@]2([H])[C@@]1(C)OC(C)(C)O2

Safety of [ 23709-41-3 ]

Application In Synthesis of [ 23709-41-3 ]

* 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 [ 23709-41-3 ]

[ 23709-41-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 492-30-8 ]
  • [ 67-64-1 ]
  • [ 23709-41-3 ]
YieldReaction ConditionsOperation in experiment
89% With sulfuric acid; at 20℃; for 16h;Cooling with ice; Inert atmosphere; 2-C-Methyl-D-ribono-1,4-lactone (50 g, 0.31 mol) was dissolved in acetone (1 L) and the solution was cooled using an ice bath followed by slow dropwise addition of conc. H2SO4(20 mL). The reaction mixture was stirred at room temperature under nitrogen for 16 h. Solid Na2CO3was added slowly to a pH of 6. The resultant mixture was filtered to remove inorganic salts and filtrate was evaporated. The oily residue was redissolved in dichloromethane and further purified by passing through a silica plug to yield 55 g of product (3.1) as off-white solids (89percent yield).
86% With sulfuric acid; at 20℃; Concentrated sulphuric acid (12 mL) was added to a suspension of <strong>[492-30-8](3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyldihydrofuran-2(3H)-one</strong> (100g, 616 mmol) in acetone (1200 mL). The mixture was stirred at room temperature overnight. The pH was then adjusted to pH 8.0 with concentrated ammonia and the mixture was filtered and concentrated in vacuo. The residue obtained was partitioned between ether and water. The organic layer was successively washed brine, dried (MgSO4), and concentrated in vacuo to give 107 g (86percent) of the alcohol as a yellow oil that solidified overnight. Rf 0.42 (1:1 iso-hexane:EtOAc); 1H NMR (CDCl3) delta 1.40 (s, 3H), 1.42 (s, 3H), 1.64 (s, 3H), 2.87 (br s, 1H, OH), 3.80 (m, 2H), 3.97 (m, 2H), 4.53 (m, 2H).
With sulfuric acid; at 20℃; for 3h; To a stirred suspension of 285-1 (300 g, 1.86 mol) in acetone (4 L) was added conc.H2SO4 (56 mL) dropwiseat RT. The mixture was stirred at RT for 3 h. The mixture was neutralized with solid NaHCO3 and filtered.The filtrate was evaporated under reduced pressure to give 285-2 (381 g, crude) as a colorless oil, which wasused for the next step without further purification
With sulfuric acid; at 20℃; for 3h; To a stirred suspension of 278-1(300 g, 1.86 mol) in acetone (4 pL) was added conc. H2S04 (56 mE) dropwise at RT. The mixture was stirred at R.T. for 3 h. The mixture was neutralized with solid NaHCO3 and filtered. The filtrate was evaporated under reduced pressure to give 278-2 (381 g, crude) as a colorless oil, which was used for the next step without further purification.

  • 2
  • [ 492-30-8 ]
  • [ 77-76-9 ]
  • [ 23709-41-3 ]
  • 3
  • [ 492-30-8 ]
  • [ 116-11-0 ]
  • [ 23709-41-3 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; In Isopropyl acetate; at 15 - 20℃; for 21h; Lactone B20.0 g lactone A (123.4 mmol) is suspended in 200 mL iPrOAc and to this mixture is added 65 muL H2SO4 (1.23 mmol, 0.01 equiv.). This mixture is cooled to 15 °C. To the cooled mixture is added 11.8mL 2-methoxypropene (123.4 mmol, 1.0 equiv.) over a period of 2 h. Upon completion of addition the mixture is allowed to stir for 12 h at 15 °C. Following age, the mixture is wanned to 20 °C and another 6.0 mL 2-methoxypropene (0.5 equiv) is added to the reaction mixture. The mixture is aged with stirring at 20 °C for an additionl 7 h. Following age, The solids are removed by filtration, rinsed with 100 mL iPrOAc. The combined organic washes are washed l with 100 mL water, and the organic layer is concentrated to a colorless oil. This oil is diluted with 100 mL heptane, and upon concentration affords colorless solids, which are collected by filtration, and rinsed with 100 mL heptane giving 8.36 g (36percent yield) of desired compound , (M+H)/Z - 203.
  • 4
  • [ 492-30-8 ]
  • [ 23709-41-3 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; In acetone; at 20℃; for 3h; To a stirred suspension of 287-1 (300 g, 1.86 mol) in acetone (4 L) was added conc.H2SO4 (56 mL) dropwise at RT. The mixture was stirred at RT for 3 h. The mixture was neutralized with solid NaHCO3 and filtered. The filtrate was evaporated under reduced pressure to give 287-2 (381 g, crude) as a colorless oil, which was used for the next step without further purification.
 

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