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1H-Isoindole-1,3(2H)-dione, 2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]-

Base Information Edit
  • Chemical Name:1H-Isoindole-1,3(2H)-dione, 2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]-
  • CAS No.:374808-54-5
  • Molecular Formula:C25H31NO5
  • Molecular Weight:425.525
  • Hs Code.:
  • Mol file:374808-54-5.mol
1H-Isoindole-1,3(2H)-dione,
2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]-

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1H-Isoindole-1,3(2H)-dione, 2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]- Edit
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Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]-

There total 9 articles about 1H-Isoindole-1,3(2H)-dione, 2-[2-[4-(6-hydroxyhexyl)-2,5-dimethoxyphenyl]-1-methylethyl]- 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 sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 18h;
DOI:10.3390/71100777
Guidance literature:
Multi-step reaction with 6 steps
1.1: 94 percent / conc. H2SO4 / 18 h / Heating
2.1: 33 percent / zinc amalgam; conc. HCl / methanol / 3 h / Heating
3.1: phosphorus oxychloride / 2 h / Heating
3.2: 35 percent / H2O / 18 h / 20 °C
4.1: 35 percent / ammonium acetate / acetic acid / 4 h / Heating
5.1: 66 percent / lithium aluminum hydride / diethyl ether / 48 h / Heating
6.1: 95 percent / sodium bicarbonate / tetrahydrofuran; H2O / 18 h / 20 °C
With ammonium acetate; hydrogenchloride; amalgamated zinc; lithium aluminium tetrahydride; sulfuric acid; sodium hydrogencarbonate; trichlorophosphate; In tetrahydrofuran; methanol; diethyl ether; water; acetic acid; 3.1: Vilsmeier-Haack formylation;
DOI:10.3390/71100777
Guidance literature:
Multi-step reaction with 8 steps
1.1: aluminum chloride / nitrobenzene / 23 h / 0 - 20 °C
2.1: 11.4 g / 3 M NaOH
3.1: 94 percent / conc. H2SO4 / 18 h / Heating
4.1: 33 percent / zinc amalgam; conc. HCl / methanol / 3 h / Heating
5.1: phosphorus oxychloride / 2 h / Heating
5.2: 35 percent / H2O / 18 h / 20 °C
6.1: 35 percent / ammonium acetate / acetic acid / 4 h / Heating
7.1: 66 percent / lithium aluminum hydride / diethyl ether / 48 h / Heating
8.1: 95 percent / sodium bicarbonate / tetrahydrofuran; H2O / 18 h / 20 °C
With ammonium acetate; hydrogenchloride; sodium hydroxide; amalgamated zinc; lithium aluminium tetrahydride; aluminium trichloride; sulfuric acid; sodium hydrogencarbonate; trichlorophosphate; In tetrahydrofuran; methanol; diethyl ether; water; acetic acid; nitrobenzene; 1.1: Friedel-Crafts acylation / 5.1: Vilsmeier-Haack formylation;
DOI:10.3390/71100777
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