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4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal

Base Information Edit
  • Chemical Name:4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal
  • CAS No.:367951-89-1
  • Molecular Formula:C32H42O5
  • Molecular Weight:506.682
  • Hs Code.:
  • Mol file:367951-89-1.mol
4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal

Synonyms:4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal

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Chemical Property of 4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal Edit
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Technology Process of 4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal

There total 12 articles about 4-(3'α-benzyloxy-15'β-hydroxy-5'β-estran-17'β-yl)furan-2-carboxyaldehyde ethylene acetal 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 hydrogen; sodium acetate; Lindlar's catalyst; In tetrahydrofuran; methanol; for 6h; under 2585.74 Torr;
DOI:10.1021/jm0505819
Guidance literature:
Multi-step reaction with 9 steps
1.1: 3.0 g / NaBH4 / methanol; tetrahydrofuran / 20 °C
2.1: 78 percent / NaH / toluene / 6 h / Heating
3.1: pyridinium tribromide / tetrahydrofuran / 20 h / 4 °C
4.1: t-BuOK / benzene; dimethylsulfoxide / 20 h / 60 °C
5.1: 3.4 g / pyridinium p-toluenesulfonate; H2O / acetone
6.1: n-BuLi / tetrahydrofuran / 0.5 h / -70 °C
6.2: 40 percent / tetrahydrofuran / 1 h / -70 °C
7.1: 96 percent / pyridine; dimethylaminopyridine / 20 °C
8.1: 54 percent / CaCO3; H2O / acetone / 72 h / Heating
9.1: 99 percent / NaOAc; H2 / Pd/CaCO3 / tetrahydrofuran; methanol / 6 h / 2585.74 Torr
With pyridine; dmap; sodium tetrahydroborate; n-butyllithium; potassium tert-butylate; water; hydrogen; sodium acetate; pyridinium p-toluenesulfonate; sodium hydride; pyridinium hydrobromide perbromide; calcium carbonate; Lindlar's catalyst; In tetrahydrofuran; methanol; dimethyl sulfoxide; acetone; toluene; benzene;
DOI:10.1021/jm0505819
Guidance literature:
Multi-step reaction with 8 steps
1.1: 78 percent / NaH / toluene / 6 h / Heating
2.1: pyridinium tribromide / tetrahydrofuran / 20 h / 4 °C
3.1: t-BuOK / benzene; dimethylsulfoxide / 20 h / 60 °C
4.1: 3.4 g / pyridinium p-toluenesulfonate; H2O / acetone
5.1: n-BuLi / tetrahydrofuran / 0.5 h / -70 °C
5.2: 40 percent / tetrahydrofuran / 1 h / -70 °C
6.1: 96 percent / pyridine; dimethylaminopyridine / 20 °C
7.1: 54 percent / CaCO3; H2O / acetone / 72 h / Heating
8.1: 99 percent / NaOAc; H2 / Pd/CaCO3 / tetrahydrofuran; methanol / 6 h / 2585.74 Torr
With pyridine; dmap; n-butyllithium; potassium tert-butylate; water; hydrogen; sodium acetate; pyridinium p-toluenesulfonate; sodium hydride; pyridinium hydrobromide perbromide; calcium carbonate; Lindlar's catalyst; In tetrahydrofuran; methanol; dimethyl sulfoxide; acetone; toluene; benzene;
DOI:10.1021/jm0505819
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