ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside
CAS No.:1253183-66-2
Molecular Formula:C₃₅H₃₅ClO₇S
Molecular Weight:635.178
Hs Code.:

Synonyms:ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

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Chemical Property of ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

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Technology Process of ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

There total 1 articles about ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside 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: 87.0%

: 1163704-54-8
ethyl 2-O-benzoyl-3-O-benzyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

: 541-88-8
Chloroacetic anhydride

: 1253183-66-2
ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

Guidance literature:: With triethylamine; In dichloromethane; at -30 ℃; for 0.5h; Inert atmosphere;
DOI:10.1016/j.tet.2010.08.004

Reference yield: 81.0%

: 1253183-66-2
ethyl 2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-1-thio-β-D-glucopyranoside

: 85193-92-6
methyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

: 1253183-68-4
methyl [2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-4-O-(1-naphthylmethyl)-β-D-glucopyranosyl]-(1->4)-(2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside)

Guidance literature:: With methyl trifluoromethanesulfonate; In dichloromethane; at 0 - 20 ℃; Molecular sieve; Inert atmosphere;
DOI:10.1016/j.tet.2010.08.004