Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

Base Information

Chemical Name:Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside
CAS No.:226982-82-7
Molecular Formula:C₃₄H₃₈Cl₃NO₁₂S
Molecular Weight:791.1
Hs Code.:

Synonyms:Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

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Chemical Property of Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

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Technology Process of Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

There total 4 articles about Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside 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: 64.0%

: 143570-52-9
ethyl 2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

: 226982-79-2
2-O-Acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl trichloroacetimidate

: 226982-82-7
Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: With 4 A molecular sieve; boron trifluoride diethyl etherate; In dichloromethane; at -78 ℃;
DOI:10.1055/s-1999-2736

Reference yield:

: 2-O-Acetyl-4-O-benzoyl-α/β-L-rhamnopyranose

: 226982-82-7
Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / DBU / CH₂Cl₂ / 20 °C

2: 64 percent / 4 Angstroem molecular sieves; BF₃*OEt₂ / CH₂Cl₂ / 0.5 h / -78 °C

With 4 A molecular sieve; boron trifluoride diethyl etherate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; 1: Addition / 2: Etherification;
DOI:10.1039/a909218h

Reference yield:

: 183613-29-8
allyl 2-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside

: 226982-82-7
Ethyl 2-O-acetyl-4-O-benzoyl-3-O-trichloroacetimidoyl-α-L-rhamnopyranosyl-(1->3)-2-O-acetyl-4-O-benzoyl-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / PdCl₂ / methanol / Ambient temperature

2: 89 percent / DBU / CH₂Cl₂ / Ambient temperature

3: 64 percent / BF₃*Et₂O, 4 Angstroem molecular sieves / CH₂Cl₂ / -78 °C

With 4 A molecular sieve; boron trifluoride diethyl etherate; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium dichloride; In methanol; dichloromethane;
DOI:10.1055/s-1999-2736