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5-((S)-5-Methyl-heptyl)-benzene-1,3-diol

Base Information
  • Chemical Name:5-((S)-5-Methyl-heptyl)-benzene-1,3-diol
  • CAS No.:220170-14-9
  • Molecular Formula:C14H22O2
  • Molecular Weight:222.327
  • Hs Code.:
5-((S)-5-Methyl-heptyl)-benzene-1,3-diol

Synonyms:5-((S)-5-Methyl-heptyl)-benzene-1,3-diol

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Chemical Property of 5-((S)-5-Methyl-heptyl)-benzene-1,3-diol
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Technology Process of 5-((S)-5-Methyl-heptyl)-benzene-1,3-diol

There total 5 articles about 5-((S)-5-Methyl-heptyl)-benzene-1,3-diol 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 boron tribromide; In dichloromethane; at 0 - 25 ℃;
DOI:10.1016/S0968-0896(98)80014-X
Guidance literature:
Multi-step reaction with 5 steps
1.1: 96 percent / oxalyl chloride; DMSO; triethylamine / CH2Cl2 / 2.3 h / -60 - 20 °C
2.1: Mg; p-toluenesulfonic acid monohydrate; 1,2-dibromoethane / diethyl ether / 2.5 h / Heating
2.2: 56 percent / diethyl ether / 2.25 h / Heating
3.1: 79 percent / pyridine / CHCl3 / 3 h / 0 - 20 °C
4.1: 81 percent / LiAlH4 / diethyl ether / 1 h / 35 °C
5.1: 100 percent / BBr3 / CH2Cl2 / 0 - 25 °C
With pyridine; lithium aluminium tetrahydride; oxalyl dichloride; boron tribromide; toluene-4-sulfonic acid; magnesium; dimethyl sulfoxide; ethylene dibromide; triethylamine; In diethyl ether; dichloromethane; chloroform; 1.1: Oxidation / 2.1: Metallation / 2.2: Grignard reaction / 3.1: Tosylation / 4.1: Reduction / 5.1: ether cleavage;
DOI:10.1016/S0968-0896(98)80014-X
Guidance literature:
Multi-step reaction with 4 steps
1.1: Mg; p-toluenesulfonic acid monohydrate; 1,2-dibromoethane / diethyl ether / 2.5 h / Heating
1.2: 56 percent / diethyl ether / 2.25 h / Heating
2.1: 79 percent / pyridine / CHCl3 / 3 h / 0 - 20 °C
3.1: 81 percent / LiAlH4 / diethyl ether / 1 h / 35 °C
4.1: 100 percent / BBr3 / CH2Cl2 / 0 - 25 °C
With pyridine; lithium aluminium tetrahydride; boron tribromide; toluene-4-sulfonic acid; magnesium; ethylene dibromide; In diethyl ether; dichloromethane; chloroform; 1.1: Metallation / 1.2: Grignard reaction / 2.1: Tosylation / 3.1: Reduction / 4.1: ether cleavage;
DOI:10.1016/S0968-0896(98)80014-X
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