(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

Base Information

Chemical Name:(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one
CAS No.:198541-59-2
Molecular Formula:C₅₃H₈₀O₇Si
Molecular Weight:857.3
Hs Code.:

(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

Synonyms:(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

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Chemical Property of (S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

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Technology Process of (S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

There total 9 articles about (S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one 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: 50.0%

: 198541-58-1
(S)-3-[(5Z,11E,15E,19E)-(2R,8R)-2-(tert-Butyl-diphenyl-silanyloxy)-8-hydroxy-dotriaconta-5,11,15,19-tetraenyl]-5-methyl-5H-furan-2-one

: 198541-59-2
(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

Guidance literature:: With rhenium(VII) oxide; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1021/ja964273z

Reference yield:

: 198541-51-4
(6E,10E,14E)-(R)-Heptacosa-6,10,14-triene-1,3-diol

: 198541-59-2
(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

Guidance literature:: Multi-step reaction with 8 steps

1: 87 percent / diisopropylethylamine / CH₂Cl₂ / 16 h / Ambient temperature

2: diisopropylethylamine / CH₂Cl₂ / 16 h / 0 - 20 °C

3: TBAF / tetrahydrofuran / 2 h / 0 - 20 °C

4: I₂, PPh₃ / 2 h / 0 - 20 °C

5: NaHCO₃ / acetonitrile / 48 h / 45 °C

6: BuLi / tetrahydrofuran / 0 °C

7: (CH₃)3SiBr / CH₂Cl₂ / 1 h / -30 °C

8: 50 percent / Re₂O₇, trifluoroacetic anhydride / tetrahydrofuran; CH₂Cl₂ / 3 h / 0 - 20 °C

With n-butyllithium; trimethylsilyl bromide; tetrabutyl ammonium fluoride; iodine; sodium hydrogencarbonate; rhenium(VII) oxide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/ja964273z

Reference yield:

: [(2R,3R)-((3E,7E,11E)-3-Tetracosa-3,7,11-trienyl)-oxiranyl]-methanol

: 198541-59-2
(S)-3-{(E)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-7-[(2R,5R,2'R,5'S,2''S,5''R)-5''-((R)-1-hydroxy-tridecyl)-dodecahydro-[2,2';5',2'']terfuran-5-yl]-hept-5-enyl}-5-methyl-5H-furan-2-one

Guidance literature:: Multi-step reaction with 9 steps

1: 77 percent / Red-Al / tetrahydrofuran / 4 h / 0 °C

2: 87 percent / diisopropylethylamine / CH₂Cl₂ / 16 h / Ambient temperature

3: diisopropylethylamine / CH₂Cl₂ / 16 h / 0 - 20 °C

4: TBAF / tetrahydrofuran / 2 h / 0 - 20 °C

5: I₂, PPh₃ / 2 h / 0 - 20 °C

6: NaHCO₃ / acetonitrile / 48 h / 45 °C

7: BuLi / tetrahydrofuran / 0 °C

8: (CH₃)3SiBr / CH₂Cl₂ / 1 h / -30 °C

9: 50 percent / Re₂O₇, trifluoroacetic anhydride / tetrahydrofuran; CH₂Cl₂ / 3 h / 0 - 20 °C

With n-butyllithium; trimethylsilyl bromide; tetrabutyl ammonium fluoride; iodine; sodium hydrogencarbonate; rhenium(VII) oxide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; sodium bis(2-methoxyethoxy)aluminium dihydride; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/ja964273z