tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Base Information

Chemical Name:tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane
CAS No.:303039-16-9
Molecular Formula:C₂₃H₄₆O₃Si
Molecular Weight:398.702
Hs Code.:

<i>tert</i>-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Synonyms:tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Suppliers and Price of tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

There total 1 articles about tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane 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:

: 55362-80-6
9-bromononan-1-ol

: 303039-16-9
tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / PTSA / 2 h / 0 - 20 °C

2: 94 percent / acetonitrile / 38 h / 70 °C

3: 78 percent / LiHMDS / tetrahydrofuran; hexamethylphosphoric acid triamide / -78 - 20 °C

With toluene-4-sulfonic acid; lithium hexamethyldisilazane; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; acetonitrile; 1: acetalisation / 2: Substitution / 3: Wittig olefination;
DOI:10.1016/S0040-4039(00)01064-9

Reference yield: 94.0%

: 303039-16-9
tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

: 69494-16-2
12-(2-Tetrahydro-2H-pyran-2-yloxy)-3(Z)-dodecen-1-ol

Guidance literature:: With tetrabutyl ammonium fluoride; at 20 ℃; for 28h;
DOI:10.1016/S0040-4039(00)01064-9

Reference yield:

: 303039-16-9
tert-butyl-dimethyl-[12-(tetrahydro-pyran-2-yloxy)-dodec-3-enyloxy]-silane

: 298691-11-9
(6E,8Z,11Z)-(S)-20-Amino-5-(tert-butyl-diphenyl-silanyloxy)-icosa-6,8,11-trienoic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 94 percent / TBAF / 28 h / 20 °C

2: 92 percent / PPh₃; I₂; imidazole / CH₂Cl₂ / 2 h / 0 - 20 °C

3: 95 percent / acetonitrile / 48 h / 70 °C

4: 85 percent / LiHMDS / tetrahydrofuran; hexamethylphosphoric acid triamide / -78 - 20 °C

5: 75 percent / Me₂AlCl / CH₂Cl₂ / 1.5 h / -30 - 20 °C

6: 88 percent / PPh₃; I₂; imidazole / CH₂Cl₂ / 0 - 20 °C

7: 89 percent / NaN₃ / acetone / 16 h / 65 °C

8: 88 percent / PPh₃ / H₂O; tetrahydrofuran / 14 h / 20 °C

With 1H-imidazole; sodium azide; tetrabutyl ammonium fluoride; iodine; dimethylaluminum chloride; triphenylphosphine; lithium hexamethyldisilazane; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; water; acetone; acetonitrile; 1: Hydrolysis / 2: Substitution / 3: Substitution / 4: Wittig olefination / 5: acetal cleavage / 6: Substitution / 7: Substitution / 8: Reduction;
DOI:10.1016/S0040-4039(00)01064-9