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Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester

Base Information Edit
  • Chemical Name:Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester
  • CAS No.:1027419-70-0
  • Molecular Formula:C50H88O7Si2
  • Molecular Weight:857.416
  • Hs Code.:
  • Mol file:1027419-70-0.mol
Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester

Synonyms:Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester

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Chemical Property of Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester Edit
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Technology Process of Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester

There total 42 articles about Benzoic acid (E)-(1S,2S,3R,4R,8R,10R)-1-{(2S,5S,2'R,5'S)-5'-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2,5'-dimethyl-octahydro-[2,2']bifuranyl-5-ylmethyl}-2,4,8,10-tetramethyl-11-oxo-3-triisopropylsilanyloxy-undec-5-enyl ester 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:
Guidance literature:
Multi-step reaction with 19 steps
1.1: (+)-diisopropyl tartrate; titanium isopropoxide; tert-butyl hydroperoxide / CH2Cl2; decane / -20 °C
2.1: 95 percent / pyridine / CH2Cl2 / 48 h / -10 °C
3.1: perchloric acid / tetrahydrofuran; H2O / 2 h / Heating
3.2: 67 percent / 2,6-lutidine / CH2Cl2 / 1 h / -20 °C
4.1: vanadil acetylacetonate; t-butyl hydroperoxide; pyridinium para-toluenesulfonate / 4 Angstroem molecular sieve / various solvent(s); CH2Cl2; decane / 29 h / 20 °C
5.1: sodium iodide; 18-c-6 / butan-2-one / Heating
5.2: 81 percent / tributyltin hydride; AIBN / toluene / 3 h / Heating
6.1: 93 percent / triethylamine / CH2Cl2 / 3 h / -78 °C
7.1: n-butyl lithium / tetrahydrofuran; hexane / 0.5 h / -78 °C
7.2: tetrahydrofuran; hexane / 0.5 h
8.1: N-methylmorpholine N-oxide / tetrapropylammonium perruthenate / CH2Cl2 / 2 h / 20 °C
9.1: 673 mg / samarium diiodide / ethanol; tetrahydrofuran / 0.5 h / -78 °C
10.1: 86 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / H2O; CH2Cl2 / 1 h / 0 °C
11.1: 90 percent / samarium diiodide / tetrahydrofuran / 0.5 h / 0 °C
12.1: 4-dimethylaminopyridine / CH2Cl2
13.1: HCl / tetrahydrofuran / 5 h / 0 °C
14.1: 264 mg / sodium hydride / tetrahydrofuran / 0.33 h / 50 °C
15.1: 96 percent / Pd(OH)2 / ethanol; cyclohexane / 12 h / Heating
16.1: 91 percent / N-methylmorpholine N-oxide / tetrapropylammonium perruthenate / CH2Cl2 / 0.5 h / 20 °C
17.1: potassium hexamethyldisilazide / tetrahydrofuran; toluene / 0.5 h
17.2: 85 percent / tetrahydrofuran; toluene / -78 - 20 °C
18.1: 97 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / H2O; CH2Cl2 / 2 h / 0 °C
19.1: DMSO; oxalyl chloride; Et3N / CH2Cl2 / 0.92 h / -78 °C
With pyridine; titanium(IV) isopropylate; hydrogenchloride; tert.-butylhydroperoxide; dmap; n-butyllithium; perchloric acid; samarium diiodide; oxalyl dichloride; bis(acetylacetonate)oxovanadium; L-(+)-diisopropyl tartrate; 18-crown-6 ether; pyridinium p-toluenesulfonate; potassium hexamethylsilazane; sodium hydride; dimethyl sulfoxide; 4-methylmorpholine N-oxide; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium iodide; palladium dihydroxide; tetrapropylammonium perruthennate; 4 A molecular sieve; In tetrahydrofuran; decane; ethanol; hexane; dichloromethane; cyclohexane; water; toluene; butanone; 11.1: Tishchenko reaction / 17.1: Julia reaction / 19.1: Swern oxidation;
DOI:10.1021/ol025872f
Guidance literature:
Multi-step reaction with 14 steps
1.1: 93 percent / triethylamine / CH2Cl2 / 3 h / -78 °C
2.1: n-butyl lithium / tetrahydrofuran; hexane / 0.5 h / -78 °C
2.2: tetrahydrofuran; hexane / 0.5 h
3.1: N-methylmorpholine N-oxide / tetrapropylammonium perruthenate / CH2Cl2 / 2 h / 20 °C
4.1: 673 mg / samarium diiodide / ethanol; tetrahydrofuran / 0.5 h / -78 °C
5.1: 86 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / H2O; CH2Cl2 / 1 h / 0 °C
6.1: 90 percent / samarium diiodide / tetrahydrofuran / 0.5 h / 0 °C
7.1: 4-dimethylaminopyridine / CH2Cl2
8.1: HCl / tetrahydrofuran / 5 h / 0 °C
9.1: 264 mg / sodium hydride / tetrahydrofuran / 0.33 h / 50 °C
10.1: 96 percent / Pd(OH)2 / ethanol; cyclohexane / 12 h / Heating
11.1: 91 percent / N-methylmorpholine N-oxide / tetrapropylammonium perruthenate / CH2Cl2 / 0.5 h / 20 °C
12.1: potassium hexamethyldisilazide / tetrahydrofuran; toluene / 0.5 h
12.2: 85 percent / tetrahydrofuran; toluene / -78 - 20 °C
13.1: 97 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / H2O; CH2Cl2 / 2 h / 0 °C
14.1: DMSO; oxalyl chloride; Et3N / CH2Cl2 / 0.92 h / -78 °C
With hydrogenchloride; dmap; n-butyllithium; samarium diiodide; oxalyl dichloride; potassium hexamethylsilazane; sodium hydride; dimethyl sulfoxide; 4-methylmorpholine N-oxide; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium dihydroxide; tetrapropylammonium perruthennate; In tetrahydrofuran; ethanol; hexane; dichloromethane; cyclohexane; water; toluene; 6.1: Tishchenko reaction / 12.1: Julia reaction / 14.1: Swern oxidation;
DOI:10.1021/ol025872f
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