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7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III

Base Information
  • Chemical Name:7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III
  • CAS No.:849213-10-1
  • Molecular Formula:C39H46O12
  • Molecular Weight:706.787
  • Hs Code.:
7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III

Synonyms:7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III

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Chemical Property of 7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III
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Technology Process of 7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III

There total 11 articles about 7,9-anisaldehyde acetal-9-desoxo-10-epi-baccatin III which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With lithium borohydride; In tetrahydrofuran; at -13 - 0 ℃; for 7.25h; Cooling with ice/water/ammonium chloride;
Guidance literature:
Multi-step reaction with 8 steps
1: water; hydrazine / Isopropyl acetate / 1 h / 20 °C
2: dmap / dichloromethane / 3 h / 20 °C
3: tetra-n-propylammonium perruthenate.; 4-methylmorpholine N-oxide / dichloromethane / 22 h / 20 °C
4: sodium tetrahydroborate / methanol; ethanol / 5 h / 0 °C
5: dmap / dichloromethane / 15 h / 20 °C
6: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C
7: toluene-4-sulfonic acid / dichloromethane / 0.75 h / 20 °C
8: lithium borohydride / tetrahydrofuran / 7.25 h / -13 - 0 °C / Cooling with ice/water/ammonium chloride
With dmap; sodium tetrahydroborate; lithium borohydride; tetra-n-propylammonium perruthenate.; tetrabutyl ammonium fluoride; water; 4-methylmorpholine N-oxide; hydrazine; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; Isopropyl acetate;
Guidance literature:
Multi-step reaction with 5 steps
1: sodium tetrahydroborate / methanol; ethanol / 5 h / 0 °C
2: triethylamine / dichloromethane / 20 °C
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C
4: toluene-4-sulfonic acid / dichloromethane / 0.75 h / 20 °C
5: lithium borohydride / tetrahydrofuran / 7.25 h / -13 - 0 °C / Cooling with ice/water/ammonium chloride
With sodium tetrahydroborate; lithium borohydride; tetrabutyl ammonium fluoride; triethylamine; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane;
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