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C26H25FO5S

Base Information Edit
C<sub>26</sub>H<sub>25</sub>FO<sub>5</sub>S

Synonyms:C26H25FO5S

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C26H25FO5S Edit
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Technology Process of C26H25FO5S

There total 1 articles about C26H25FO5S 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:
(2-(4-fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene); With isopropylmagnesium chloride; lithium chloride; In tetrahydrofuran; for 1h; Cooling with ice;
((3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(morpholin-4-yl)methanone; In tetrahydrofuran; for 1h;
Guidance literature:
C26H25FO5S; With cerium(III) chloride heptahydrate; In methanol; at 20 ℃; for 0.333333h;
With sodium tetrahydroborate; In methanol; at -78 ℃; for 1h;
With methanol; water;
Guidance literature:
Multi-step reaction with 6 steps
1.1: cerium(III) chloride heptahydrate / methanol / 0.33 h / 20 °C
1.2: 1 h / -78 °C
2.1: acetic acid / water / 15 h / 100 °C
2.2: 2 h / 20 °C / Cooling with ice
3.1: hydrogen bromide; acetic acid / 1 h / 20 °C / Cooling with ice
4.1: thiourea / acetonitrile / 1 h / Reflux
5.1: triethylamine / 1 h / 20 °C
6.1: urea hydrogen peroxide adduct / acetonitrile; methanol / 20 °C
With cerium(III) chloride heptahydrate; hydrogen bromide; urea hydrogen peroxide adduct; acetic acid; triethylamine; thiourea; In methanol; water; acetonitrile;
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