(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

Base Information

Chemical Name:(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol
CAS No.:122624-90-2
Molecular Formula:C₂₅H₄₂O₄Si
Molecular Weight:434.692
Hs Code.:

Synonyms:(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

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Chemical Property of (2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

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Technology Process of (2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

There total 5 articles about (2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol 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:

: 3587-60-8
Benzyloxymethyl chloride

: 122624-90-2
(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / NEt(i-Pr)2 / 1,2-dichloro-ethane / 18 h / 75 °C

2: 100 percent / DIBAL / CH₂Cl₂; hexane / 0.75 h / -78 °C

3: 82 percent / benzene / 18 h / 70 °C

4: 100 percent / 1,2-dichloro-ethane / 6 h / 60 °C

5: 100 percent / DIBAL / CH₂Cl₂; hexane / 0.5 h / -78 °C

With diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In hexane; dichloromethane; 1,2-dichloro-ethane; benzene;
DOI:10.1021/ja00199a030

Reference yield:

: 122624-85-5
(4S,5R)-5-(4'-methyl-3'-pentenyl)-4-hydroxy-5-methyldihydrofuran-2-one

: 122624-90-2
(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / NEt(i-Pr)2 / 1,2-dichloro-ethane / 18 h / 75 °C

2: 100 percent / DIBAL / CH₂Cl₂; hexane / 0.75 h / -78 °C

3: 82 percent / benzene / 18 h / 70 °C

4: 100 percent / 1,2-dichloro-ethane / 6 h / 60 °C

5: 100 percent / DIBAL / CH₂Cl₂; hexane / 0.5 h / -78 °C

With diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; In hexane; dichloromethane; 1,2-dichloro-ethane; benzene;
DOI:10.1021/ja00199a030

Reference yield:

: 122624-87-7,122624-88-8
(4S,5R)-4-<(Benzyloxy)methoxy>-2-hydroxy-5-methyl-5-(4-methyl-3-pentenyl)tetrahydrofuran

: 122624-90-2
(2E,5S,6R)-5-<(Benzyloxy)methoxy>-2,6,10-trimethyl-6-(trimethylsiloxy)-2,9-undecadien-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / benzene / 18 h / 70 °C

2: 100 percent / 1,2-dichloro-ethane / 6 h / 60 °C

3: 100 percent / DIBAL / CH₂Cl₂; hexane / 0.5 h / -78 °C

With diisobutylaluminium hydride; In hexane; dichloromethane; 1,2-dichloro-ethane; benzene;
DOI:10.1021/ja00199a030