(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

Base Information

Chemical Name:(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene
CAS No.:781642-41-9
Molecular Formula:C₂₉H₄₇IO₃Si
Molecular Weight:598.68
Hs Code.:

Synonyms:(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

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Chemical Property of (1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

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Technology Process of (1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

There total 7 articles about (1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene 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: 92.0%

: 102-92-1,17082-09-6
Cinnamoyl chloride

: 781642-40-8
(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-oct-1-en-6-ol

: 781642-41-9
(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 48h;
DOI:10.1021/ol048574m

Reference yield:

: 781642-33-9
(3S,4R,5R,6S)-8-(benzyloxy)-3,5-dimethyl-6-(triisopropylsilyloxy)-oct-1-en-4-ol

: 781642-41-9
(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

Guidance literature:: Multi-step reaction with 6 steps

1: 84 percent / i-Pr₂NEt; DMAP / CH₂Cl₂ / 18 h / 0 - 20 °C

2: 86 percent / H₂ / Pd/C / methanol / 24 h

3: 98 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

4: CrCl₂ / dioxane; tetrahydrofuran / 20 h / 0 - 20 °C

5: 75 percent / BCl₃ / CH₂Cl₂; hexane / 2 h / -78 °C

6: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 48 h / 0 - 20 °C

With chromium dichloride; dmap; oxalyl dichloride; hydrogen; boron trichloride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane; 3: Swern oxidation / 4: Takai's iodoolefination;
DOI:10.1021/ol048574m

Reference yield:

: 781642-37-3
(3S,4R,5R,6S)-8-(benzyloxy)-3,5-dimethyl-4-methoxymethoxy-6-(triisopropylsilyloxy)-oct-1-ene

: 781642-41-9
(1E,4S,5R,6R,7S)-5,7-dimethyl-1-iodo-4-(triisopropylsilyloxy)-6-[(2E)-3-phenylacryloxy]oct-1-ene

Guidance literature:: Multi-step reaction with 5 steps

1: 86 percent / H₂ / Pd/C / methanol / 24 h

2: 98 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

3: CrCl₂ / dioxane; tetrahydrofuran / 20 h / 0 - 20 °C

4: 75 percent / BCl₃ / CH₂Cl₂; hexane / 2 h / -78 °C

5: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 48 h / 0 - 20 °C

With chromium dichloride; dmap; oxalyl dichloride; hydrogen; boron trichloride; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane; 2: Swern oxidation / 3: Takai's iodoolefination;
DOI:10.1021/ol048574m