8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

Base Information

Chemical Name:8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione
CAS No.:135366-17-5
Molecular Formula:C₃₂H₄₄N₂O₅Si
Molecular Weight:564.797
Hs Code.:

Synonyms:8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

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Chemical Property of 8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

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Technology Process of 8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

There total 8 articles about 8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione 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: 98.0%

: 135366-16-4
8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-<(phenylselenyl)methyl>-1-methylbicyclo<4.2.2>decane-7,9-dione

: 135366-17-5
8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

Guidance literature:: With dihydrogen peroxide; In tetrahydrofuran; for 1h; Heating;

Reference yield:

: 135366-12-0
(Z)-11,13-bis(p-methoxybenzyl)-11,13-diaza-9-methyl-2-oxabicyclo<7.2.2>tridec-4-ene-10,12-dione

: 135366-17-5
8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C

2: 95 percent / 2,6-lutidine / CH₂Cl₂ / 1.5 h

3: 1.) triethylamine, methanesulfonyl chloride, 2.) NaBH₄ / 1.) THF, 0 deg C, 1 h, 2.) ethanol, 80 deg C, 7.5 h

4: 98 percent / 30percent H₂O₂ / tetrahydrofuran / 1 h / Heating

With 2,6-dimethylpyridine; sodium tetrahydroborate; n-butyllithium; dihydrogen peroxide; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; hexane; dichloromethane;

Reference yield:

: 135366-10-8,135416-39-6
(Z)-1,4-bis(p-methoxybenzyl)-3-(6'-hydroxy-4'-hexenyl)-6-methoxy-2,5-piperazinedione

: 135366-17-5
8,10-bis(p-methoxybenzyl)-8,10-diaza-6-<(tert-butyldimethylsilyl)oxy>-5-methylene-1-methylbicyclo<4.2.2>decane-7,9-dione

Guidance literature:: Multi-step reaction with 6 steps

1: 37 percent / p-toluenesulfonic acid, pyridinium p-toluenesulfonate / CH₂Cl₂ / 70 h / Heating

2: 1.) lithium hexamethyldisilazide, HMPA / 1.) THF, 10 min, 2.) THF, 1.5 h

3: 84 percent / n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C

4: 95 percent / 2,6-lutidine / CH₂Cl₂ / 1.5 h

5: 1.) triethylamine, methanesulfonyl chloride, 2.) NaBH₄ / 1.) THF, 0 deg C, 1 h, 2.) ethanol, 80 deg C, 7.5 h

6: 98 percent / 30percent H₂O₂ / tetrahydrofuran / 1 h / Heating

With 2,6-dimethylpyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; n-butyllithium; dihydrogen peroxide; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; methanesulfonyl chloride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane;