(3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal

Base Information

• Chemical Name: (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal
• CAS No.: 212507-90-9
• Molecular Formula: C₃₀H₅₂O₄Si
• Molecular Weight: 504.826
• Mol file: 212507-90-9.mol

Synonyms:(3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal

Chemical Property of (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal

There total 19 articles about (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal 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:

((2S,3S)-3-(1-(benzyloxy)-2-methylpropan-2-yl)oxiran-2-yl)methanol (130199-57-4) → (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal (212507-90-9)

Guidance literature:

Multi-step reaction with 18 steps

1: 1.) (COCl)2, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) CH₂Cl₂, 0 deg C, 1 h

2: NaH / tetrahydrofuran / 1.) 0 deg C, 1 h, 2.) 0 deg C, 30 min

3: 87 percent / H₂O / hexane; 1,2-dichloro-ethane / -30 °C

4: 2,6-lutidine / CH₂Cl₂ / 0.75 h

6: 93 percent / (R,R)-diisopropyl tartrate, 4 Angstroem molecular sieves / toluene / 1.) -78 deg C, 3 h, 2.) r.t., 12 h

7: TBAF / tetrahydrofuran / 0.5 h

8: TsOH / 0.25 h

9: 1.) catecholborane, 2.) H₂O₂, NaOH / 1.) (PPh₃)3RhCl / 1.) THF, 45 min

10: 1.) (COCl)2, DMSO, 2.) Et₃N

11: NaH / tetrahydrofuran / 4 h

12: H₂ / 10percent Pd/C / ethanol; ethyl acetate / 5 h

13: tetrahydrofuran / 3 h

14: HCl, H₂O / tetrahydrofuran / 3 h / 50 °C

15: 90 percent / TsOH / benzene / 0.5 h

16: 94 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / -78 °C

17: 75 percent / DIBAL-H / CH₂Cl₂ / 1.5 h / -78 - -15 °C

18: 1.) (COCl)2, DMSO, 2.) Et₃N

With 2,6-dimethylpyridine; hydrogenchloride; sodium hydroxide; oxalyl dichloride; L-(+)-diisopropyl tartrate; 4 A molecular sieve; tetrabutyl ammonium fluoride; water; hydrogen; dihydrogen peroxide; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; benzo[1,3,2]dioxaborole; palladium on activated charcoal; Wilkinson's catalyst; In tetrahydrofuran; ethanol; hexane; dichloromethane; ethyl acetate; 1,2-dichloro-ethane; toluene; benzene;

DOI:10.1039/a802947d

Reference yield:

(E)-5-(benzyloxy)-4,4-dimethylpent-2-en-1-ol (121352-87-2) → (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal (212507-90-9)

Guidance literature:

Multi-step reaction with 19 steps

1: diethyl L-tartrate, Ti(O-i-Pr)4, t-BuOOH, 4 Angstroem molecular sieves / CH₂Cl₂ / 1.) -40 deg C, 8 h, 2.) -10 deg C, 8 h

2: 1.) (COCl)2, DMSO, 2.) Et₃N / 1.) CH₂Cl₂, -78 deg C, 1 h, 2.) CH₂Cl₂, 0 deg C, 1 h

3: NaH / tetrahydrofuran / 1.) 0 deg C, 1 h, 2.) 0 deg C, 30 min

4: 87 percent / H₂O / hexane; 1,2-dichloro-ethane / -30 °C

5: 2,6-lutidine / CH₂Cl₂ / 0.75 h

7: 93 percent / (R,R)-diisopropyl tartrate, 4 Angstroem molecular sieves / toluene / 1.) -78 deg C, 3 h, 2.) r.t., 12 h

8: TBAF / tetrahydrofuran / 0.5 h

9: TsOH / 0.25 h

10: 1.) catecholborane, 2.) H₂O₂, NaOH / 1.) (PPh₃)3RhCl / 1.) THF, 45 min

11: 1.) (COCl)2, DMSO, 2.) Et₃N

12: NaH / tetrahydrofuran / 4 h

13: H₂ / 10percent Pd/C / ethanol; ethyl acetate / 5 h

14: tetrahydrofuran / 3 h

15: HCl, H₂O / tetrahydrofuran / 3 h / 50 °C

16: 90 percent / TsOH / benzene / 0.5 h

17: 94 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / -78 °C

18: 75 percent / DIBAL-H / CH₂Cl₂ / 1.5 h / -78 - -15 °C

19: 1.) (COCl)2, DMSO, 2.) Et₃N

With 2,6-dimethylpyridine; titanium(IV) isopropylate; hydrogenchloride; tert.-butylhydroperoxide; sodium hydroxide; oxalyl dichloride; diethyl (2R,3R)-tartrate; L-(+)-diisopropyl tartrate; 4 A molecular sieve; tetrabutyl ammonium fluoride; water; hydrogen; dihydrogen peroxide; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; benzo[1,3,2]dioxaborole; palladium on activated charcoal; Wilkinson's catalyst; In tetrahydrofuran; ethanol; hexane; dichloromethane; ethyl acetate; 1,2-dichloro-ethane; toluene; benzene;

DOI:10.1039/a802947d

Reference yield:

(2R,3S)-3-(2-Benzyloxy-1,1-dimethyl-ethyl)-oxirane-2-carbaldehyde → (3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-enal (212507-90-9)

Guidance literature:

Multi-step reaction with 17 steps

1: NaH / tetrahydrofuran / 1.) 0 deg C, 1 h, 2.) 0 deg C, 30 min

2: 87 percent / H₂O / hexane; 1,2-dichloro-ethane / -30 °C

3: 2,6-lutidine / CH₂Cl₂ / 0.75 h

5: 93 percent / (R,R)-diisopropyl tartrate, 4 Angstroem molecular sieves / toluene / 1.) -78 deg C, 3 h, 2.) r.t., 12 h

6: TBAF / tetrahydrofuran / 0.5 h

7: TsOH / 0.25 h

8: 1.) catecholborane, 2.) H₂O₂, NaOH / 1.) (PPh₃)3RhCl / 1.) THF, 45 min

9: 1.) (COCl)2, DMSO, 2.) Et₃N

10: NaH / tetrahydrofuran / 4 h

11: H₂ / 10percent Pd/C / ethanol; ethyl acetate / 5 h

12: tetrahydrofuran / 3 h

13: HCl, H₂O / tetrahydrofuran / 3 h / 50 °C

14: 90 percent / TsOH / benzene / 0.5 h

15: 94 percent / 2,6-lutidine / CH₂Cl₂ / 4 h / -78 °C

16: 75 percent / DIBAL-H / CH₂Cl₂ / 1.5 h / -78 - -15 °C

17: 1.) (COCl)2, DMSO, 2.) Et₃N

With 2,6-dimethylpyridine; hydrogenchloride; sodium hydroxide; oxalyl dichloride; L-(+)-diisopropyl tartrate; 4 A molecular sieve; tetrabutyl ammonium fluoride; water; hydrogen; dihydrogen peroxide; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; benzo[1,3,2]dioxaborole; palladium on activated charcoal; Wilkinson's catalyst; In tetrahydrofuran; ethanol; hexane; dichloromethane; ethyl acetate; 1,2-dichloro-ethane; toluene; benzene;

DOI:10.1039/a802947d

upstream raw materials:

(3R,4S,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,2,4,6,10-pentamethyl-undec-10-en-1-ol

(E)-5-(benzyloxy)-4,4-dimethylpent-2-en-1-ol

((2S,3S)-3-(1-(benzyloxy)-2-methylpropan-2-yl)oxiran-2-yl)methanol

(3R,4R,5S,6S)-2,2,4,6,10-Pentamethyl-undec-10-ene-1,3,5-triol

Downstream raw materials:

epothilone B

(4S,7R,8S,9S,13Z,16S,1'E)-4,8-di-tert-butyldimethylsilyloxy-5,5,7,9,13-pentamethyl-16-[1-methyl-2-(2-methyl-1,3-thiazol-4-yl)-1-ethenyl]-1-oxa-13-cyclohexadecene-2,6-dione

epothilone D

(3S,5R,6S,7S,8S)-7-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-5-(4-methoxy-benzyloxy)-4,4,6,8,12-pentamethyl-tridec-12-enoic acid (S)-1-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-but-3-enyl ester