1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

Base Information

Chemical Name:1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol
CAS No.:760987-52-8
Molecular Formula:C₃₆H₃₈O₇
Molecular Weight:582.694
Hs Code.:

Synonyms:1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

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Chemical Property of 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

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Technology Process of 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

There total 4 articles about 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol 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:

Reference yield: 93.0%

: 356067-96-4
1,5-anhydro-3-O-benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

: 760987-49-3
4-(3,4-dimethoxyphenyl)benzyl bromide

: 760987-52-8
1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 4h;
DOI:10.1039/b407324j

Reference yield:

: 873-75-6
4-bromobenzenemethanol

: 760987-52-8
1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / K₃PO₄; Bu₄NBr / Pd(OAc)2 / ethanol

2: 91 percent / PBr₃ / tetrahydrofuran / 2 h / 0 - 20 °C

3: 93 percent / NaH / dimethylformamide / 4 h / 0 - 20 °C

With potassium phosphate; tetrabutylammomium bromide; phosphorus tribromide; sodium hydride; palladium diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 1: Suzuki-Miyaura coupling;
DOI:10.1039/b407324j

Reference yield:

: 122775-35-3
3,4-Dimethoxyphenylboronic acid

: 760987-52-8
1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / K₃PO₄; Bu₄NBr / Pd(OAc)2 / ethanol

2: 91 percent / PBr₃ / tetrahydrofuran / 2 h / 0 - 20 °C

3: 93 percent / NaH / dimethylformamide / 4 h / 0 - 20 °C

With potassium phosphate; tetrabutylammomium bromide; phosphorus tribromide; sodium hydride; palladium diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 1: Suzuki-Miyaura coupling;
DOI:10.1039/b407324j