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7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol

Base Information Edit
  • Chemical Name:7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol
  • CAS No.:478490-27-6
  • Molecular Formula:C36H52O7S
  • Molecular Weight:628.871
  • Hs Code.:
  • Mol file:478490-27-6.mol
7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol

Synonyms:7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol

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Chemical Property of 7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol Edit
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Technology Process of 7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol

There total 12 articles about 7α-[9-(4-methylphenylsulfonyloxy)nonyl]-3-O-methoxymethylestra-1,3,5(10)-triene-3,16β,17β-triol 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 12 steps
1.1: 95 percent / imidazole / tetrahydrofuran / 2 h / 20 °C
2.1: Mg / tetrahydrofuran / 2 h / Heating
2.2: 37 percent / CuI / tetrahydrofuran / 0.67 h
3.1: 81 percent / pyridinium chlorochromate / CH2Cl2 / 2 h / 0 - 20 °C
4.1: aq. AcOH / tetrahydrofuran / 50 °C
5.1: 2.28 g / N,N-diisopropylethylamine / CH2Cl2 / 0.5 h / 0 °C
6.1: 68 percent / CuBr2; LiBr / acetonitrile / 0.5 h / Heating
7.1: 66 percent / H2SO4 / 4 h / Heating
8.1: 81 percent / Pb(OAc)4 / acetic acid / 3.5 h
9.1: Li(t-BuO)3AlH / tetrahydrofuran / 1 h
10.1: 0.64 g / aq. K2CO3 / methanol / 2 h / 20 °C
11.1: 91 percent / NaH / tetrahydrofuran / 1 h
12.1: 62 percent / DMAP / CH2Cl2 / 15 h / 0 - 20 °C
With 1H-imidazole; lead(IV) acetate; dmap; sulfuric acid; sodium hydride; potassium carbonate; magnesium; acetic acid; lithium tri-t-butoxyaluminum hydride; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; lithium bromide; copper(ll) bromide; In tetrahydrofuran; methanol; dichloromethane; acetic acid; acetonitrile;
DOI:10.1039/b205571f
Guidance literature:
Multi-step reaction with 11 steps
1.1: Mg / tetrahydrofuran / 2 h / Heating
1.2: 37 percent / CuI / tetrahydrofuran / 0.67 h
2.1: 81 percent / pyridinium chlorochromate / CH2Cl2 / 2 h / 0 - 20 °C
3.1: aq. AcOH / tetrahydrofuran / 50 °C
4.1: 2.28 g / N,N-diisopropylethylamine / CH2Cl2 / 0.5 h / 0 °C
5.1: 68 percent / CuBr2; LiBr / acetonitrile / 0.5 h / Heating
6.1: 66 percent / H2SO4 / 4 h / Heating
7.1: 81 percent / Pb(OAc)4 / acetic acid / 3.5 h
8.1: Li(t-BuO)3AlH / tetrahydrofuran / 1 h
9.1: 0.64 g / aq. K2CO3 / methanol / 2 h / 20 °C
10.1: 91 percent / NaH / tetrahydrofuran / 1 h
11.1: 62 percent / DMAP / CH2Cl2 / 15 h / 0 - 20 °C
With lead(IV) acetate; dmap; sulfuric acid; sodium hydride; potassium carbonate; magnesium; acetic acid; lithium tri-t-butoxyaluminum hydride; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; lithium bromide; copper(ll) bromide; In tetrahydrofuran; methanol; dichloromethane; acetic acid; acetonitrile;
DOI:10.1039/b205571f
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