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(4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde

Base Information
  • Chemical Name:(4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde
  • CAS No.:261775-46-6
  • Molecular Formula:C26H36O4Si
  • Molecular Weight:440.655
  • Hs Code.:
(4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde

Synonyms:(4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde

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Chemical Property of (4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde
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Technology Process of (4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde

There total 6 articles about (4R,5R,6S)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-[1,3]dioxane-4-carbaldehyde 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:
Guidance literature:
Multi-step reaction with 5 steps
1: tert-butyl hydroperoxide; 4-Angstroem molecular sieves / diisopropyl (-)-D-tartrate; Ti(iPrO)4 / CH2Cl2 / 0.42 h / -20 °C
2: Cp2TiCl; cyclohexa-1,4-diene / tetrahydrofuran / 8 h / -20 - 20 °C
3: camphorsulfonic acid / CH2Cl2 / 1 h / 0 °C
4: H2 / Pd/C / ethyl acetate / 2 h / 20 °C / 760.05 Torr
5: SO3-pyridine complex; Et3N / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C
With tert.-butylhydroperoxide; bis(cyclopentadienyl)titanium (III) chloride; pyridine-SO3 complex; cyclohexa-1,4-diene; 4 A molecular sieve; camphor-10-sulfonic acid; hydrogen; triethylamine; titanium(IV) isopropylate; palladium on activated charcoal; D-(-)-diisopropyl tartrate; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; ethyl acetate; 1: Sharpless asymmetric epoxidation;
DOI:10.1021/jo010131y
Guidance literature:
Multi-step reaction with 2 steps
1: H2 / Pd/C / ethyl acetate / 2 h / 20 °C / 760.05 Torr
2: SO3-pyridine complex; Et3N / CH2Cl2; dimethylsulfoxide / 1 h / 0 °C
With pyridine-SO3 complex; hydrogen; triethylamine; palladium on activated charcoal; In dichloromethane; dimethyl sulfoxide; ethyl acetate;
DOI:10.1021/jo010131y
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