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Chemical Structure| 2887-07-2 Chemical Structure| 2887-07-2

Structure of 2887-07-2

Chemical Structure| 2887-07-2

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Product Details of [ 2887-07-2 ]

CAS No. :2887-07-2
Formula : C21H24O11
M.W : 452.41
SMILES Code : O(C(C)=O)[C@@H]1[C@@H](OC(C)=O)[C@H](OC2=CC=C(C=O)C=C2)O[C@H](COC(C)=O)[C@@H]1OC(C)=O
MDL No. :N/A

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Application In Synthesis of [ 2887-07-2 ]

* 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 [ 2887-07-2 ]

[ 2887-07-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2887-07-2 ]
  • [ 62499-27-8 ]
YieldReaction ConditionsOperation in experiment
96.2% With sodium tetrahydroborate; sodium methylate; In methanol; at 50℃; To the methanol (400 g) was added 4-formylphenyl-2,3,4,6-O-tetraacetyl-beta-D-glucopyranoside (0.2 mol, 90.5 g) 3.0g), PH value was measured, the reaction was heated to 50 C for 7 hours, evaporated under reduced pressure to dry methanol and transesterification of methyl acetate, methanol (400g) was added, a small amount of sodium methylate to adjust the PH is alkaline, then slowly added Sodium borohydride (0.07 mol, 2.65 g) was detected by TLC. After the reaction was completed, activated carbon was decolored and the resulting metal salt such as sodium acetate was removed and concentrated to dryness under reduced pressure to give a white solid which was recrystallized from 95% Cycle applied many times) to give 55.1g of white crystalline solid gastrodin, yield 96.2%, melting point 154.5-155.5
63.5% With methanol; potassium borohydride; at 58℃; for 0.5h;Industrial scale; Example 6Take 1kg tetraacetyl. Add 3.5L anhydrous methanol. Heat to 58 C reflux. Add potassium borohydride then undergo reduction reaction. After reacting for 30 min. Take sample then add, dropwise, chromogenic agent. When ared color does not appear (if red color is still apparent, continue adding potassium borohydride to undergo reaction). Concentrate recovered anhydrous ethanol to concentrated solution 1L. Undergo thin liquid chromatography to determine reaction completion. Add 3L anhydrous ethanol. Concentrate to concentrated solution 2L. Undergo thin liquid chromatography to determine reaction completion. Add 4L anhydrous ethanol to concentrated solution 2L. Quench potassium borohydride using 20% aqueous sulfuric acid. Make the pH of the alcohol solution to pH 7. Allow to stand for 8h. Eliminate precipitated solids. Concentrate to separate out gastrodin. Stop concentration. Allow concentrated solution to stand for 8h at room temperature to crystallize. Crumble bulk solids, dry, obtain 0.635 kg gastrodin. The gastrodin underwent tests to be in line with the national standard. In terms of tetraacetyl, mass yield 63.5%, molar yield 97.3%.
 

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