C₃₅H₄₈O₁₀

Base Information

Chemical Name:C₃₅H₄₈O₁₀
CAS No.:1352816-13-7
Molecular Formula:C₃₅H₄₈O₁₀
Molecular Weight:628.76
Hs Code.:

C<sub>35</sub>H<sub>48</sub>O<sub>10</sub>

Synonyms:C₃₅H₄₈O₁₀

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Chemical Property of C₃₅H₄₈O₁₀

Chemical Property:

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Technology Process of C₃₅H₄₈O₁₀

There total 11 articles about C₃₅H₄₈O₁₀ 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:

Reference yield:

: C₃₈H₅₆O₁₀Si

: 1352816-12-6
C₃₃H₄₄O₉

: 1352816-13-7
C₃₅H₄₈O₁₀

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1002/anie.201104681

Reference yield:

: 1352816-09-1
C₅₀H₆₆O₉Si

: 1352816-13-7
C₃₅H₄₈O₁₀

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine; dmap / dichloromethane / 1 h / 0 - 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 10 h / 20 °C

3: pyridine; tributylphosphine / tetrahydrofuran / 1.5 h / 20 °C / Inert atmosphere

4: dihydrogen peroxide / dichloromethane; water / 29 h / 20 °C / pH 7 / aq. phosphate buffer

5: cerium(III) chloride heptahydrate; oxalic acid / acetonitrile / 2 h / 20 °C

6: dichloromethane / 1.5 h / 20 °C

7: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

8: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C

With pyridine; dmap; tributylphosphine; cerium(III) chloride heptahydrate; tetrabutyl ammonium fluoride; dihydrogen peroxide; oxalic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.1002/anie.201104681

Reference yield:

: 1352816-07-9
C₅₀H₆₄O₈Si

: 1352816-13-7
C₃₅H₄₈O₁₀

Guidance literature:: Multi-step reaction with 10 steps

1.1: o-xylene / 20 h / 165 °C / Inert atmosphere

2.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 24 h / 20 °C

2.2: NaBO₃*4H₂O / 3 h / 20 °C

3.1: pyridine; dmap / dichloromethane / 1 h / 0 - 20 °C

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 10 h / 20 °C

5.1: pyridine; tributylphosphine / tetrahydrofuran / 1.5 h / 20 °C / Inert atmosphere

6.1: dihydrogen peroxide / dichloromethane; water / 29 h / 20 °C / pH 7 / aq. phosphate buffer

7.1: cerium(III) chloride heptahydrate; oxalic acid / acetonitrile / 2 h / 20 °C

8.1: dichloromethane / 1.5 h / 20 °C

9.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

10.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C

With pyridine; dmap; tributylphosphine; cerium(III) chloride heptahydrate; tetrabutyl ammonium fluoride; dihydrogen peroxide; oxalic acid; N-ethyl-N,N-diisopropylamine; 9-bora-bicyclo[3.3.1]nonane; In tetrahydrofuran; dichloromethane; o-xylene; water; acetonitrile; 2.1: Hydroboration reaction;
DOI:10.1002/anie.201104681