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C37H46O5

Base Information
  • Chemical Name:C37H46O5
  • CAS No.:1374425-57-6
  • Molecular Formula:C37H46O5
  • Molecular Weight:570.769
  • Hs Code.:
C<sub>37</sub>H<sub>46</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C37H46O5
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Chemical Property of C37H46O5
Chemical Property:
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Technology Process of C37H46O5

There total 25 articles about C37H46O5 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 lead(IV) tetraacetate; In dichloromethane; at 20 ℃; for 0.166667h; Inert atmosphere;
DOI:10.1002/ejoc.201101629
Guidance literature:
Multi-step reaction with 20 steps
1.1: methanol; diethyl ether; toluene / 0.25 h / Inert atmosphere
2.1: lithium aluminium tetrahydride / tetrahydrofuran; dichloromethane / 0.5 h / 0 °C / Inert atmosphere
3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere
3.2: 16 h / 20 °C / Inert atmosphere
4.1: toluene-4-sulfonic acid / water; acetone / 0.5 h / 20 °C
5.1: triethylamine / dichloromethane / 0.75 h / 0 °C / Inert atmosphere
6.1: oxygen; palladium diacetate / dimethyl sulfoxide / 16 h / 20 - 80 °C
7.1: iodine; magnesium / tetrahydrofuran / 2 h / 70 °C / Inert atmosphere
7.2: 0.5 h / -78 °C / Inert atmosphere
7.3: 5 h / -78 °C / Inert atmosphere
8.1: toluene-4-sulfonic acid / acetone / 0.5 h / 20 °C / Inert atmosphere
9.1: n-butyllithium; lithium diisopropyl amide / tetrahydrofuran; cyclohexane / 1 h / -78 °C / Inert atmosphere
9.2: 3 h / -78 °C / Inert atmosphere
10.1: pyridine; dihydrogen peroxide / dichloromethane; water / 0.5 h / 0 - 20 °C
11.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.25 h / -78 °C / Inert atmosphere
12.1: 1,2-dichloro-benzene / 1 h / 220 °C / Microwave irradiation; Inert atmosphere
13.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
13.2: 0.5 h / -78 - 20 °C / Inert atmosphere
14.1: water; iodine / tetrahydrofuran / 16 h / 20 °C
15.1: triethyl borane; tri-n-butyl-tin hydride / hexane; toluene / 1 h / -78 °C / Air
16.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere
17.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / -50 °C / Inert atmosphere
17.2: 3 h / -50 °C / Inert atmosphere
18.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 3 h / 20 °C / Inert atmosphere
19.1: bis-triphenylphosphine-palladium(II) chloride; tri-n-butyl-tin hydride / tetrahydrofuran / Inert atmosphere
19.2: 5 h / 20 °C
20.1: lead(IV) tetraacetate / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
With pyridine; bis-triphenylphosphine-palladium(II) chloride; lithium aluminium tetrahydride; n-butyllithium; triethyl borane; water; dihydrogen peroxide; iodine; oxygen; tri-n-butyl-tin hydride; lead(IV) tetraacetate; palladium diacetate; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; toluene-4-sulfonic acid; magnesium; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; cyclohexane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 1,2-dichloro-benzene; acetone; toluene; mineral oil;
DOI:10.1002/ejoc.201101629
Guidance literature:
Multi-step reaction with 22 steps
1.1: triethylamine / dichloromethane / 3 h / -78 °C / Inert atmosphere
2.1: ozone / dichloromethane / 3 h / -78 °C
2.2: 4 h / 20 °C / Inert atmosphere
3.1: methanol; diethyl ether; toluene / 0.25 h / Inert atmosphere
4.1: lithium aluminium tetrahydride / tetrahydrofuran; dichloromethane / 0.5 h / 0 °C / Inert atmosphere
5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere
5.2: 16 h / 20 °C / Inert atmosphere
6.1: toluene-4-sulfonic acid / water; acetone / 0.5 h / 20 °C
7.1: triethylamine / dichloromethane / 0.75 h / 0 °C / Inert atmosphere
8.1: oxygen; palladium diacetate / dimethyl sulfoxide / 16 h / 20 - 80 °C
9.1: iodine; magnesium / tetrahydrofuran / 2 h / 70 °C / Inert atmosphere
9.2: 0.5 h / -78 °C / Inert atmosphere
9.3: 5 h / -78 °C / Inert atmosphere
10.1: toluene-4-sulfonic acid / acetone / 0.5 h / 20 °C / Inert atmosphere
11.1: n-butyllithium; lithium diisopropyl amide / tetrahydrofuran; cyclohexane / 1 h / -78 °C / Inert atmosphere
11.2: 3 h / -78 °C / Inert atmosphere
12.1: pyridine; dihydrogen peroxide / dichloromethane; water / 0.5 h / 0 - 20 °C
13.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.25 h / -78 °C / Inert atmosphere
14.1: 1,2-dichloro-benzene / 1 h / 220 °C / Microwave irradiation; Inert atmosphere
15.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
15.2: 0.5 h / -78 - 20 °C / Inert atmosphere
16.1: water; iodine / tetrahydrofuran / 16 h / 20 °C
17.1: triethyl borane; tri-n-butyl-tin hydride / hexane; toluene / 1 h / -78 °C / Air
18.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere
19.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / -50 °C / Inert atmosphere
19.2: 3 h / -50 °C / Inert atmosphere
20.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 3 h / 20 °C / Inert atmosphere
21.1: bis-triphenylphosphine-palladium(II) chloride; tri-n-butyl-tin hydride / tetrahydrofuran / Inert atmosphere
21.2: 5 h / 20 °C
22.1: lead(IV) tetraacetate / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
With pyridine; bis-triphenylphosphine-palladium(II) chloride; lithium aluminium tetrahydride; n-butyllithium; triethyl borane; water; dihydrogen peroxide; iodine; oxygen; tri-n-butyl-tin hydride; lead(IV) tetraacetate; palladium diacetate; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; toluene-4-sulfonic acid; ozone; magnesium; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; cyclohexane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 1,2-dichloro-benzene; acetone; toluene; mineral oil;
DOI:10.1002/ejoc.201101629
upstream raw materials:

C25H30O3

C35H52O3Si2

C32H44O3Si

C32H42O3Si

Downstream raw materials:

C37H44O5

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