6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

Base Information

Chemical Name:6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate
CAS No.:144367-26-0
Molecular Formula:C₃₇H₃₆Cl₃NO₁₁
Molecular Weight:777.052
Hs Code.:

Synonyms:6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

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Technology Process of 6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

There total 12 articles about 6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate 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: 89.0%

: 545-06-2
trichloroacetonitrile

: 6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α/β-D-glucopyranoside

: 144367-26-0
6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane;
DOI:10.1016/S0008-6215(00)90971-6

Reference yield:

: 2872-65-3,14581-81-8,17042-40-9,84380-06-3,105260-62-6
p-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

: 144367-26-0
6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 7 steps

1: NaOMe / methanol / 8 h / pH 10

2: pyridine / 4.5 h / 0 °C

3: pyridine / Ambient temperature

4: p-toluenesulfonic acid / acetonitrile; H₂O / 5 h / pH 3

5: 2-chloro-1-methylpyridinium iodide, 1,4-diazabicyclo<2.2.2>octane / 1,2-dichloro-ethane / 0.33 h

6: 88 percent / ammonium cerium(IV) nitrate / toluene; acetonitrile; H₂O / 0.5 h

7: 89 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / CH₂Cl₂

With 1,4-diaza-bicyclo[2.2.2]octane; ammonium cerium(IV) nitrate; 2-chloro-1-methyl-pyridinium iodide; sodium methylate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In pyridine; methanol; dichloromethane; water; 1,2-dichloro-ethane; toluene; acetonitrile;
DOI:10.1016/S0008-6215(98)00125-6

Reference yield:

: 144367-33-9
4-methoxyphenyl 6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-β-D-glucopyranoside

: 144367-26-0
6-O-levulinoyl-2,3,4-tri-O-p-toluoyl-α-D-glucopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / ammonium cerium(IV) nitrate / toluene; acetonitrile; H₂O / 0.5 h

2: 89 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / CH₂Cl₂

With ammonium cerium(IV) nitrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; water; toluene; acetonitrile;
DOI:10.1016/S0008-6215(98)00125-6