8,13-Pentadecadiynoic acid, 12-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-10-[[(1,1-dimethylethyl)diphenyl silyl]oxy]-15-iodo-5-(1-methylethenyl)-3-oxo-, 1,1-dimethylethyl ester, (5S)-

Base Information

• Chemical Name: 8,13-Pentadecadiynoic acid, 12-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-10-[[(1,1-dimethylethyl)diphenyl silyl]oxy]-15-iodo-5-(1-methylethenyl)-3-oxo-, 1,1-dimethylethyl ester, (5S)-
• CAS No.: 392334-80-4
• Molecular Formula: C44H63IO5Si2
• Molecular Weight: 855.057
• Mol file: 392334-80-4.mol

Synonyms:

Chemical Property of 8,13-Pentadecadiynoic acid, 12-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-10-[[(1,1-dimethylethyl)diphenyl silyl]oxy]-15-iodo-5-(1-methylethenyl)-3-oxo-, 1,1-dimethylethyl ester, (5S)-

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 8,13-Pentadecadiynoic acid, 12-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-10-[[(1,1-dimethylethyl)diphenyl silyl]oxy]-15-iodo-5-(1-methylethenyl)-3-oxo-, 1,1-dimethylethyl ester, (5S)-

There total 14 articles about 8,13-Pentadecadiynoic acid, 12-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-10-[[(1,1-dimethylethyl)diphenyl silyl]oxy]-15-iodo-5-(1-methylethenyl)-3-oxo-, 1,1-dimethylethyl ester, (5S)- 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:

t-butyl (5S)-12-(t-butyldimethylsilyloxy)-10-(t-butyldiphenylsilyloxy)-15-hydroxy-5-isopropenyl-3-keto-8,13-pentadecadiynoate (392334-79-1) → t-butyl (5S)-12-(t-butyldimethylsilyloxy)-10-(t-butyldiphenylsilyloxy)-5-isopropenyl-3-keto-15-iodo-8,13-pentadecadiynoate (392334-80-4)

Guidance literature:

With 1H-imidazole; iodine; triphenylphosphine; In diethyl ether; benzene; at 20 ℃; for 0.75h;

DOI:10.1021/jo016048s

Reference yield:

(-)-perillyl alcohol (536-59-4,18457-55-1) → t-butyl (5S)-12-(t-butyldimethylsilyloxy)-10-(t-butyldiphenylsilyloxy)-5-isopropenyl-3-keto-15-iodo-8,13-pentadecadiynoate (392334-80-4)

Guidance literature:

Multi-step reaction with 14 steps

1.1: 98 percent / VO(acac)2; tert-butyl hydroperoxide / CH₂Cl₂; various solvent(s) / 1 h / 0 °C

2.1: H₅IO₆ / tetrahydrofuran / 0.25 h / 0 °C

2.2: 75 percent / p-TsOH / methanol / Heating

3.1: 97 percent / DIBAL-H / various solvent(s) / 1 h / -78 °C

4.1: 85 percent / K₂CO₃ / methanol / 2 h / 20 °C

5.1: BuLi / tetrahydrofuran; various solvent(s) / 1 h / -40 °C

5.2: LiBr / tetrahydrofuran; various solvent(s) / 0.25 h

5.3: 84 percent / tetrahydrofuran; various solvent(s) / -40 - -30 °C

6.1: 97 percent / imidazole / dimethylformamide / 20 °C

7.1: 96 percent / pyridinium p-toluenesulfonate / methanol / 20 °C

8.1: 100 percent / Dess-Martin periodinane; NaHCO₃ / CH₂Cl₂ / 1.5 h

9.1: BuLi / tetrahydrofuran; various solvent(s) / 1 h / -40 °C

9.2: LiBr / tetrahydrofuran; various solvent(s) / 0.25 h

9.3: 88 percent / tetrahydrofuran; various solvent(s) / -40 - -30 °C

10.1: 99 percent / p-TsOH / acetone; H₂O / 48 h / 20 °C

11.1: 91 percent / imidazole / dimethylformamide / 20 °C

12.1: 85 percent / SnCl₂ / CH₂Cl₂ / 2 h / 20 °C

13.1: 85 percent / DDQ / CH₂Cl₂ / 6 h / 20 °C / pH 7

14.1: I₂; triphenylphosphine; imidazole / diethyl ether; benzene / 0.75 h / 20 °C

With 1H-imidazole; tert.-butylhydroperoxide; n-butyllithium; bis(acetylacetonate)oxovanadium; iodine; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; toluene-4-sulfonic acid; periodic acid; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; tin(ll) chloride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; acetone; benzene;

DOI:10.1021/jo016048s

Reference yield:

((4S)-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptan-1-yl)methanol (190718-78-6) → t-butyl (5S)-12-(t-butyldimethylsilyloxy)-10-(t-butyldiphenylsilyloxy)-5-isopropenyl-3-keto-15-iodo-8,13-pentadecadiynoate (392334-80-4)

Guidance literature:

Multi-step reaction with 13 steps

1.1: H₅IO₆ / tetrahydrofuran / 0.25 h / 0 °C

1.2: 75 percent / p-TsOH / methanol / Heating

2.1: 97 percent / DIBAL-H / various solvent(s) / 1 h / -78 °C

3.1: 85 percent / K₂CO₃ / methanol / 2 h / 20 °C

4.1: BuLi / tetrahydrofuran; various solvent(s) / 1 h / -40 °C

4.2: LiBr / tetrahydrofuran; various solvent(s) / 0.25 h

4.3: 84 percent / tetrahydrofuran; various solvent(s) / -40 - -30 °C

5.1: 97 percent / imidazole / dimethylformamide / 20 °C

6.1: 96 percent / pyridinium p-toluenesulfonate / methanol / 20 °C

7.1: 100 percent / Dess-Martin periodinane; NaHCO₃ / CH₂Cl₂ / 1.5 h

8.1: BuLi / tetrahydrofuran; various solvent(s) / 1 h / -40 °C

8.2: LiBr / tetrahydrofuran; various solvent(s) / 0.25 h

8.3: 88 percent / tetrahydrofuran; various solvent(s) / -40 - -30 °C

9.1: 99 percent / p-TsOH / acetone; H₂O / 48 h / 20 °C

10.1: 91 percent / imidazole / dimethylformamide / 20 °C

11.1: 85 percent / SnCl₂ / CH₂Cl₂ / 2 h / 20 °C

12.1: 85 percent / DDQ / CH₂Cl₂ / 6 h / 20 °C / pH 7

13.1: I₂; triphenylphosphine; imidazole / diethyl ether; benzene / 0.75 h / 20 °C

With 1H-imidazole; n-butyllithium; iodine; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; toluene-4-sulfonic acid; periodic acid; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; tin(ll) chloride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; acetone; benzene;

DOI:10.1021/jo016048s

upstream raw materials:

t-butyl (5S)-12-(t-butyldimethylsilyloxy)-10-(t-butyldiphenylsilyloxy)-15-hydroxy-5-isopropenyl-3-keto-8,13-pentadecadiynoate

(-)-perillyl alcohol

((4S)-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptan-1-yl)methanol

(S)-7,7-dimethoxy-5-isopropenyl-1-heptyne

Downstream raw materials:

(13S)-2-t-butoxycarbonyl-6-(t-butyldimethylsilyloxy)-8-(t-butyldiphenylsilyloxy)-13-isopropenyl-4,9-cyclotetradecadiynone

(13S)-2-t-butoxycarbonyl-6-hydroxy-8-(t-butyldiphenylsilyloxy)-13-isopropenyl-4,9-cyclotetradecadiynone

(13S)-2-t-butoxycarbonyl-8-(t-butyldiphenylsilyloxy)-13-isopropenyl-4,9-cyclotetradecadiyne-1,6-dione

5-(tert-butyl-diphenyl-silanyloxy)-10-isopropenyl-3-oxo-15-oxa-bicyclo[10.2.1]pentadeca-1⁽¹⁴⁾,12-dien-6-yne-13-carboxylic acid tert-butyl ester