methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

Base Information

Chemical Name:methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside
CAS No.:37091-14-8
Molecular Formula:C₂₂H₂₅NO₅
Molecular Weight:383.444
Hs Code.:

Synonyms:methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

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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 methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

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Technology Process of methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

There total 1 articles about methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside 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:

: 98-88-4
benzoyl chloride

: 37091-14-8
methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

Guidance literature:: Yield given. Multistep reaction;

Reference yield: 100.0%

: 37091-14-8
methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

: 138925-09-4
1,5-anhydro-3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hex-1-enitol

Guidance literature:: With camphor-10-sulfonic acid; In benzene; for 12h; Heating;

Reference yield:

: 37091-14-8
methyl 3-benzamido-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside

: 138925-10-7
Benzoic acid (1R,5R,7S,8S,9S)-9-iodo-1,7-dimethyl-3-phenyl-4,6-dioxa-2-aza-bicyclo[3.3.1]non-2-en-8-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / camphorsulfonic acid / benzene / 12 h / Heating

2: 1.) 4-A molecular sieves, 2.) I(sym-collidine)2ClO₄ / 1.) CH₂Cl₂, RT, 30 min, 2.) CH₂Cl₂, from 0 deg C to RT, 5 h

With iodonium(di-γ-collidine) perchlorate; 4 A molecular sieve; camphor-10-sulfonic acid; In benzene;