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C24H37ClO5Si

Base Information
  • Chemical Name:C24H37ClO5Si
  • CAS No.:1388153-30-7
  • Molecular Formula:C24H37ClO5Si
  • Molecular Weight:469.093
  • Hs Code.:
C<sub>24</sub>H<sub>37</sub>ClO<sub>5</sub>Si

Synonyms:C24H37ClO5Si

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Chemical Property of C24H37ClO5Si
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Technology Process of C24H37ClO5Si

There total 16 articles about C24H37ClO5Si 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: 100.0%

Guidance literature:
With N-chloro-succinimide; triphenylphosphine; methyloxirane; In dichloromethane; at 0 ℃; for 0.75h;
DOI:10.1021/ja305864z
Guidance literature:
Multi-step reaction with 3 steps
1.1: diisobutylaluminium hydride / hexane; dichloromethane / 0.5 h / -78 °C / Inert atmosphere
2.1: titanium(IV) isopropylate; (-)-diethyl tartrate / dichloromethane / 0.5 h / -20 °C / Molecular sieve
2.2: -20 °C / Molecular sieve
3.1: N-chloro-succinimide; triphenylphosphine; methyloxirane / dichloromethane / 0.75 h / 0 °C
With titanium(IV) isopropylate; N-chloro-succinimide; (-)-diethyl tartrate; diisobutylaluminium hydride; triphenylphosphine; methyloxirane; In hexane; dichloromethane; 2.1: Sharpless epoxidation / 2.2: Sharpless epoxidation;
DOI:10.1021/ja305864z
Guidance literature:
Multi-step reaction with 9 steps
1.1: camphor-10-sulfonic acid / methanol; dichloromethane / 5 h / 0 °C
2.1: sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 1 h / 0 °C
3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
3.2: 2 h / -78 - 0 °C
4.1: tetrahydrofuran / 0.5 h / 20 °C
5.1: dihydrogen peroxide; sodium hydroxide / tetrahydrofuran; water / 2 h / 0 - 20 °C
6.1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane / 1.5 h / 20 °C
6.2: 1 h / 20 °C
7.1: diisobutylaluminium hydride / hexane; dichloromethane / 0.5 h / -78 °C / Inert atmosphere
8.1: titanium(IV) isopropylate; (-)-diethyl tartrate / dichloromethane / 0.5 h / -20 °C / Molecular sieve
8.2: -20 °C / Molecular sieve
9.1: N-chloro-succinimide; triphenylphosphine; methyloxirane / dichloromethane / 0.75 h / 0 °C
With titanium(IV) isopropylate; N-chloro-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; (-)-diethyl tartrate; camphor-10-sulfonic acid; potassium tert-butylate; dihydrogen peroxide; sulfur trioxide pyridine complex; diisobutylaluminium hydride; triethylamine; triphenylphosphine; methyloxirane; sodium hydroxide; In tetrahydrofuran; methanol; hexane; dichloromethane; water; dimethyl sulfoxide; 8.1: Sharpless epoxidation / 8.2: Sharpless epoxidation;
DOI:10.1021/ja305864z
upstream raw materials:

C14H18O3

C26H25O7P

C27H48O5Si2

C21H32O5Si

Downstream raw materials:

C24H36O5Si

C24H35IO5Si

C24H37IO5Si

C56H80O8Si2

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