C₁₃H₁₉NO₆S

Base Information

Chemical Name:C₁₃H₁₉NO₆S
CAS No.:1372809-46-5
Molecular Formula:C₁₃H₁₉NO₆S
Molecular Weight:317.363
Hs Code.:

C<sub>13</sub>H<sub>19</sub>NO<sub>6</sub>S

Synonyms:C₁₃H₁₉NO₆S

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Chemical Property of C₁₃H₁₉NO₆S

Chemical Property:

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Technology Process of C₁₃H₁₉NO₆S

There total 6 articles about C₁₃H₁₉NO₆S 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:

: C₂₀H₂₅NO₆S

: 1372809-46-5
C₁₃H₁₉NO₆S

Guidance literature:: With 5%-palladium/activated carbon; ammonium formate; In methanol; at 20 - 40 ℃; for 8h; Inert atmosphere;
DOI:10.3998/ark.5550190.0013.319

Reference yield:

: C₁₆H₂₇LiO₂Si

: 1372809-46-5
C₁₃H₁₉NO₆S

Guidance literature:: Multi-step reaction with 5 steps

1: ammonium chloride / pentane; diethyl ether / 16 h / 0 - 23 °C / Inert atmosphere

2: hydrogenchloride / water; ethanol / 2 h / 90 °C / Inert atmosphere

3: triethylamine; triethylamine sulfur trioxide / dichloromethane / 48 h / 20 - 23 °C / Inert atmosphere

4: sodium tetrahydroborate / methanol / 16 h / 20 - 23 °C / Inert atmosphere

5: 5%-palladium/activated carbon; ammonium formate / methanol / 8 h / 20 - 40 °C / Inert atmosphere

With hydrogenchloride; sodium tetrahydroborate; 5%-palladium/activated carbon; ammonium formate; triethylamine sulfur trioxide; ammonium chloride; triethylamine; In methanol; diethyl ether; ethanol; dichloromethane; water; pentane;
DOI:10.3998/ark.5550190.0013.319

Reference yield:

: 1372809-43-2
(1-benzylpiperidin-4-yl)-(2-methoxy-3-triisopropylsilanyloxyphenyl)methanone

: 1372809-46-5
C₁₃H₁₉NO₆S

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / water; ethanol / 2 h / 90 °C / Inert atmosphere

2: triethylamine; triethylamine sulfur trioxide / dichloromethane / 48 h / 20 - 23 °C / Inert atmosphere

3: sodium tetrahydroborate / methanol / 16 h / 20 - 23 °C / Inert atmosphere

4: 5%-palladium/activated carbon; ammonium formate / methanol / 8 h / 20 - 40 °C / Inert atmosphere

With hydrogenchloride; sodium tetrahydroborate; 5%-palladium/activated carbon; ammonium formate; triethylamine sulfur trioxide; triethylamine; In methanol; ethanol; dichloromethane; water;
DOI:10.3998/ark.5550190.0013.319