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1H-Indole-4-acetaldehyde, 3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl ethyl)silyl]oxy]-

Base Information
  • Chemical Name:1H-Indole-4-acetaldehyde, 3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl ethyl)silyl]oxy]-
  • CAS No.:925463-63-4
  • Molecular Formula:C34H43NO5SSi
  • Molecular Weight:605.871
  • Hs Code.:
1H-Indole-4-acetaldehyde,
3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl
ethyl)silyl]oxy]-

Synonyms:

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Chemical Property of 1H-Indole-4-acetaldehyde, 3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl ethyl)silyl]oxy]-
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Technology Process of 1H-Indole-4-acetaldehyde, 3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl ethyl)silyl]oxy]-

There total 12 articles about 1H-Indole-4-acetaldehyde, 3-methyl-1-[(4-methylphenyl)sulfonyl]-7-(phenylmethoxy)-5-[[tris(1-methyl ethyl)silyl]oxy]- 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:
Multi-step reaction with 8 steps
1: 84 percent / pyridine / CH2Cl2 / 4 h / 20 °C
2: 96 percent / sodium periodate on silica gel / CH2Cl2 / 4 h
3: CH2Cl2 / 15 h / 20 °C
4: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.33 h / 0 °C
5: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C
6: osmium tetroxide; N-methylmorpholine N-oxide / tetrahydrofuran; H2O
7: sodium periodate on silica gel / CH2Cl2 / 2 h
8: 3.00 g / sulfuric acid / tetrahydrofuran / 5 h
With pyridine; sodium periodate; osmium(VIII) oxide; sulfuric acid; sodium hydride; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; water; 3: Diels-Alder reaction;
DOI:10.1021/jo062064j
Guidance literature:
Multi-step reaction with 9 steps
1: sodium borohydride; nickel(II) chloride hexahydrate / tetrahydrofuran; methanol
2: 84 percent / pyridine / CH2Cl2 / 4 h / 20 °C
3: 96 percent / sodium periodate on silica gel / CH2Cl2 / 4 h
4: CH2Cl2 / 15 h / 20 °C
5: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.33 h / 0 °C
6: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C
7: osmium tetroxide; N-methylmorpholine N-oxide / tetrahydrofuran; H2O
8: sodium periodate on silica gel / CH2Cl2 / 2 h
9: 3.00 g / sulfuric acid / tetrahydrofuran / 5 h
With pyridine; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; sulfuric acid; sodium hydride; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; water; 4: Diels-Alder reaction;
DOI:10.1021/jo062064j
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