N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

Base Information

Chemical Name:N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide
CAS No.:503306-47-6
Molecular Formula:C₇₅H₁₀₁NO₁₃
Molecular Weight:1224.63
Hs Code.:

Synonyms:N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

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Chemical Property of N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

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Technology Process of N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

There total 5 articles about N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide 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:

: 183901-63-5
2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl trichloroacetimidate

: 503306-39-6
N-(2-hydroxyethyl)-3,5-bis(hexadecyloxy)benzamide

: 503306-47-6
N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/S0968-0896(02)00266-3

Reference yield:

: 99-10-5
3,5-Dihydroxybenzoic acid

: 503306-47-6
N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: K₂CO₃ / dimethylformamide / 65 °C

1.2: 74 percent / dimethylformamide / 27 h / 65 °C

2.1: 100 percent / MeONa / CH₂Cl₂ / 14 h / 20 °C

3.1: 91 percent / dimethylformamide / 21 h / 110 °C

4.1: TMSOTf / CH₂Cl₂ / 0 - 20 °C

With trimethylsilyl trifluoromethanesulfonate; sodium methylate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(02)00266-3

Reference yield:

: 112-82-3
hexadecanyl bromide

: 503306-47-6
N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: K₂CO₃ / dimethylformamide / 65 °C

1.2: 74 percent / dimethylformamide / 27 h / 65 °C

2.1: 100 percent / MeONa / CH₂Cl₂ / 14 h / 20 °C

3.1: 91 percent / dimethylformamide / 21 h / 110 °C

4.1: TMSOTf / CH₂Cl₂ / 0 - 20 °C

With trimethylsilyl trifluoromethanesulfonate; sodium methylate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(02)00266-3