(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

Base Information

Chemical Name:(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester
CAS No.:460077-75-2
Molecular Formula:C₂₉H₄₀O₄Si
Molecular Weight:480.72
Hs Code.:

Synonyms:(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

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Chemical Property of (Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

Chemical Property:

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Technology Process of (Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

There total 6 articles about (Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl 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:

Reference yield: 88.0%

: 460077-86-5
(11S,9Z)-11-[(tert-butyldiphenylsilyl)oxy]-12-hydroxydodec-9-enoic acid methyl ester

: 460077-75-2
(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

Guidance literature:: With sodium acetate; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 1.25h;
DOI:10.1021/jo011102q

Reference yield:

: 67878-16-4
(8-methoxycarbonyloctyl)triphenylphosphonium bromide

: 460077-75-2
(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.75 h / 0 - 20 °C

1.2: 66 percent / tetrahydrofuran / 2 h / 0 °C

2.1: 90 percent / hydrochloric acid / methanol; H₂O / 4 h / 0 °C

3.1: 79 percent / triethylamine; 1,8-diazobicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 17 h / 20 °C

4.1: 88 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 22 h / 20 °C

5.1: 89 percent / pyridinium p-toluenesulfonate / ethanol / 10 h / 55 °C

6.1: 88 percent / pyridinium chlorochromate; sodium acetate / CH₂Cl₂ / 1.25 h / 20 °C

With hydrogenchloride; dmap; sodium acetate; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; pyridinium chlorochromate; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; 1.2: Wittig reaction;
DOI:10.1021/jo011102q

Reference yield:

: 460077-82-1
(4'S,9Z)-10-(2,2-dimethyl-1,3-dioxalan-4-yl)-dec-9-enoic acid methyl ester

: 460077-75-2
(Z)-(S)-11-(tert-Butyl-diphenyl-silanyloxy)-12-oxo-dodec-9-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / hydrochloric acid / methanol; H₂O / 4 h / 0 °C

2: 79 percent / triethylamine; 1,8-diazobicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 17 h / 20 °C

3: 88 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 22 h / 20 °C

4: 89 percent / pyridinium p-toluenesulfonate / ethanol / 10 h / 55 °C

5: 88 percent / pyridinium chlorochromate; sodium acetate / CH₂Cl₂ / 1.25 h / 20 °C

With hydrogenchloride; dmap; sodium acetate; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; pyridinium chlorochromate; In methanol; ethanol; dichloromethane; water;
DOI:10.1021/jo011102q