(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

Base Information

Chemical Name:(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol
CAS No.:865838-79-5
Molecular Formula:C₂₄H₃₈O₆
Molecular Weight:422.562
Hs Code.:

Synonyms:(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

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Chemical Property of (5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

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Technology Process of (5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

There total 9 articles about (5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-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: 66.0%

: 865838-76-2
(2E)-4-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-2-methylbut-2-enal

: 2622-05-1
allylmagnesium bromide

: 865838-79-5
(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

Guidance literature:: In diethyl ether; at -78 - 20 ℃; for 1.66667h;
DOI:10.1055/s-2005-869970

Reference yield:

: 865838-62-6
2-bromomethyl-1,4-diisopropoxy-3-methoxybenzene

: 865838-79-5
(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

Guidance literature:: Multi-step reaction with 6 steps

1: 62 percent / NaOH / 2.33 h / 110 °C

2: 75 percent / oxalyl chloride; Et₃N; DMSO / CH₂Cl₂ / -78 - 20 °C

3: 92 percent / toluene / 12 h / 60 °C

4: 75 percent / LiAlH₄ / diethyl ether / 2 h / 20 °C

5: 80 percent / oxalyl chloride; Et₃N; DMSO / CH₂Cl₂ / -78 - 20 °C

6: 66 percent / diethyl ether / 1.67 h / -78 - 20 °C

With sodium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane; toluene; 1: Williamson ether synthesis / 2: Swern oxidation / 3: Wittig reaction / 5: Swern oxidation;
DOI:10.1055/s-2005-869970

Reference yield:

: 865838-61-5
(3,6-diisopropoxy-2-methoxy)benzyl alcohol

: 865838-79-5
(5E)-7-[2-(3,6-diisopropoxy-2-methoxybenzyloxy)ethoxy]-5-methylhepta-1,5-dien-4-ol

Guidance literature:: Multi-step reaction with 7 steps

1: 97 percent / Ph₃P; CBr₄ / CH₂Cl₂ / 1 h / 0 °C

2: 62 percent / NaOH / 2.33 h / 110 °C

3: 75 percent / oxalyl chloride; Et₃N; DMSO / CH₂Cl₂ / -78 - 20 °C

4: 92 percent / toluene / 12 h / 60 °C

5: 75 percent / LiAlH₄ / diethyl ether / 2 h / 20 °C

6: 80 percent / oxalyl chloride; Et₃N; DMSO / CH₂Cl₂ / -78 - 20 °C

7: 66 percent / diethyl ether / 1.67 h / -78 - 20 °C

With sodium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; carbon tetrabromide; dimethyl sulfoxide; triethylamine; triphenylphosphine; In diethyl ether; dichloromethane; toluene; 2: Williamson ether synthesis / 3: Swern oxidation / 4: Wittig reaction / 6: Swern oxidation;
DOI:10.1055/s-2005-869970