(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

Base Information

Chemical Name:(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester
CAS No.:1027964-53-9
Molecular Formula:C₁₉H₂₈O₄
Molecular Weight:320.429
Hs Code.:

Synonyms:(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

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Chemical Property of (E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

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Technology Process of (E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

There total 9 articles about (E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester 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: 96.0%

: 906534-76-7
(3S,4R)-4-Benzyloxymethoxy-3,5-dimethyl-hexanal

: 21204-67-1,2605-67-6
methyl (triphenylphosphoranylidene)acetate

: 1027964-53-9
(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

Guidance literature:: In dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/jo061098o

Reference yield:

: 906534-75-6
(3S,4R)-4-benzyloxymethoxy-3,5-dimethylhexan-1-ol

: 1027964-53-9
(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

2: 96 percent / CH₂Cl₂ / 18 h / 20 °C

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; 1: Swern oxidation / 2: Wittig olefination;
DOI:10.1021/jo061098o

Reference yield:

: 3587-60-8
Benzyloxymethyl chloride

: 1027964-53-9
(E)-(5S,6R)-6-benzyloxymethoxy-5,7-dimethyloct-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: 85 percent / iPr₂NEt / CH₂Cl₂

2.1: 92 percent / DIBAL-H / CH₂Cl₂ / 4 h / -78 °C

3.1: 97 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

4.1: 91 percent / CH₂Cl₂ / 18 h / 20 °C

5.1: CuI; LiBr / tetrahydrofuran / 0.33 h / -15 °C

5.2: 96 percent / TMSCl / tetrahydrofuran / 3 h / -78 °C

6.1: 93 percent / DIBAL-H / CH₂Cl₂ / 4 h / -78 °C

7.1: 81 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

8.1: 96 percent / CH₂Cl₂ / 18 h / 20 °C

With copper(l) iodide; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium bromide; In tetrahydrofuran; dichloromethane; 3.1: Swern oxidation / 4.1: Wittig olefination / 7.1: Swern oxidation / 8.1: Wittig olefination;
DOI:10.1021/jo061098o