benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

Base Information

Chemical Name:benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside
CAS No.:111266-71-8
Molecular Formula:C₆₆H₁₀₉NO₁₁
Molecular Weight:1092.59
Hs Code.:

benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

Synonyms:benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

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Chemical Property of benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

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Technology Process of benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

There total 8 articles about benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-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:

: 28715-21-1,3422-31-9
(R)-3-hydroxytetradecanoic acid

: 111266-71-8
benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / ethyl acetate / 6 h / Ambient temperature

2: diisopropylethylamine / CH₂Cl₂ / Ambient temperature

3: zinc dust / acetic acid / 50 °C

4: DCC, DMAP / CH₂Cl₂ / Ambient temperature

With dmap; triethylamine; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; zinc; In dichloromethane; acetic acid; ethyl acetate;
DOI:10.1016/0008-6215(87)80207-0

Reference yield:

: 87357-65-1
(3R)-3-hydroxytetradecanoic acid phenacyl ester

: 111266-71-8
benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: diisopropylethylamine / CH₂Cl₂ / Ambient temperature

2: zinc dust / acetic acid / 50 °C

3: DCC, DMAP / CH₂Cl₂ / Ambient temperature

With dmap; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; zinc; In dichloromethane; acetic acid;
DOI:10.1016/0008-6215(87)80207-0

Reference yield:

: 3587-60-8
Benzyloxymethyl chloride

: 111266-71-8
benzyl 3-O-<(3R)-3-(benzyloxymethoxy)tetradecanoyl>-2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: diisopropylethylamine / CH₂Cl₂ / Ambient temperature

2: zinc dust / acetic acid / 50 °C

3: DCC, DMAP / CH₂Cl₂ / Ambient temperature

With dmap; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; zinc; In dichloromethane; acetic acid;
DOI:10.1016/0008-6215(87)80207-0