C₅₉H₆₁ClO₂₄

Base Information

Chemical Name:C₅₉H₆₁ClO₂₄
CAS No.:311349-80-1
Molecular Formula:C₅₉H₆₁ClO₂₄
Molecular Weight:1189.57
Hs Code.:

C<sub>59</sub>H<sub>61</sub>ClO<sub>24</sub>

Synonyms:C₅₉H₆₁ClO₂₄

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Chemical Property of C₅₉H₆₁ClO₂₄

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Technology Process of C₅₉H₆₁ClO₂₄

There total 8 articles about C₅₉H₆₁ClO₂₄ 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:

: 127514-28-7
Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside

: 311349-80-1
C₅₉H₆₁ClO₂₄

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / pyridine / CH₂Cl₂ / 0.67 h / 0 °C

2: 98 percent / aq. H₂SO₄ / dioxane / 1 h / 80 °C

3: 98 percent / pyridine / CH₂Cl₂ / 2 h / 20 °C

4: 92 percent / thiourea; 2,6-lutidine / methanol; CH₂Cl₂ / 16 h / Heating

5: 62 percent / 4 Angstroem molecular sieves; TMSOTf / CH₂Cl₂ / 1 h

With pyridine; 2,6-dimethylpyridine; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; sulfuric acid; thiourea; In 1,4-dioxane; methanol; dichloromethane; 1: Acylation / 2: Hydrolysis / 3: Acetylation / 4: Substitution / 5: Condensation;

Reference yield:

: 311349-72-1
Benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-(2-chloro-acetoxy)-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester

: 311349-80-1
C₅₉H₆₁ClO₂₄

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / pyridine / CH₂Cl₂ / 2 h / 20 °C

2: 92 percent / thiourea; 2,6-lutidine / methanol; CH₂Cl₂ / 16 h / Heating

3: 62 percent / 4 Angstroem molecular sieves; TMSOTf / CH₂Cl₂ / 1 h

With pyridine; 2,6-dimethylpyridine; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; thiourea; In methanol; dichloromethane; 1: Acetylation / 2: Substitution / 3: Condensation;

Reference yield:

: 311349-73-2
4,6-Di-O-acetyl-2-O-benzoyl-3-O-chloroacetyl-α-D-glucopyranoside

: 311349-80-1
C₅₉H₆₁ClO₂₄

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / thiourea; 2,6-lutidine / methanol; CH₂Cl₂ / 16 h / Heating

2: 62 percent / 4 Angstroem molecular sieves; TMSOTf / CH₂Cl₂ / 1 h

With 2,6-dimethylpyridine; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; thiourea; In methanol; dichloromethane; 1: Substitution / 2: Condensation;