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C22H24O5

Base Information Edit
C<sub>22</sub>H<sub>24</sub>O<sub>5</sub>

Synonyms:C22H24O5

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C22H24O5 Edit
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Technology Process of C22H24O5

There total 9 articles about C22H24O5 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 methanol; lithium borohydride; In tetrahydrofuran; diethyl ether; for 5h;
DOI:10.1021/ol303482k
Guidance literature:
Multi-step reaction with 9 steps
1.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 24 h / Reflux
2.1: 2 h / 200 °C
3.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 24 h / Reflux
4.1: (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II) / tetrahydrofuran / 3 h / Reflux
5.1: 2,6-dimethylpyridine; osmium(VIII) oxide; sodium periodate / 1,4-dioxane; water; tert-butyl alcohol / 0.5 h
6.1: sodium tetrahydroborate; methanol / tetrahydrofuran / 0.08 h / 0 °C
7.1: phosphorus tribromide / tetrahydrofuran; dichloromethane / 4.5 h / 0 °C
8.1: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C
8.2: 0.5 h / -78 °C
9.1: methanol; lithium borohydride / tetrahydrofuran; diethyl ether / 5 h
With 2,6-dimethylpyridine; methanol; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; lithium borohydride; (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); sodium hexamethyldisilazane; phosphorus tribromide; tetra-(n-butyl)ammonium iodide; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; diethyl ether; dichloromethane; water; acetone; tert-butyl alcohol;
DOI:10.1021/ol303482k
Guidance literature:
Multi-step reaction with 10 steps
1.1: potassium carbonate / acetone / 12 h / 20 °C
2.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 24 h / Reflux
3.1: 2 h / 200 °C
4.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 24 h / Reflux
5.1: (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II) / tetrahydrofuran / 3 h / Reflux
6.1: 2,6-dimethylpyridine; osmium(VIII) oxide; sodium periodate / 1,4-dioxane; water; tert-butyl alcohol / 0.5 h
7.1: sodium tetrahydroborate; methanol / tetrahydrofuran / 0.08 h / 0 °C
8.1: phosphorus tribromide / tetrahydrofuran; dichloromethane / 4.5 h / 0 °C
9.1: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C
9.2: 0.5 h / -78 °C
10.1: methanol; lithium borohydride / tetrahydrofuran; diethyl ether / 5 h
With 2,6-dimethylpyridine; methanol; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; lithium borohydride; (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); sodium hexamethyldisilazane; phosphorus tribromide; tetra-(n-butyl)ammonium iodide; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; diethyl ether; dichloromethane; water; acetone; tert-butyl alcohol;
DOI:10.1021/ol303482k
upstream raw materials:

eugenin

eugenin

C14H14O4

C14H14O4

Downstream raw materials:

C22H22O5

C23H24O5

C33H46O7Si

C33H46O7Si

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