Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

Base Information

Chemical Name:Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester
CAS No.:135253-85-9
Molecular Formula:C₂₃H₂₈N₂O₁₀
Molecular Weight:492.483
Hs Code.:

Synonyms:Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

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Chemical Property of Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

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Technology Process of Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

There total 4 articles about Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester 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: 95.0%

: 65907-85-9
p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

: 814-68-6,25189-84-8
acryloyl chloride

: 135253-85-9
Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃;
DOI:10.1039/c39910000536

Reference yield:

: 13089-27-5,13089-23-1
p-nitrophenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside

: 135253-85-9
Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium formate / 10percent Pd/C / methanol / 0.08 h / Heating

2: 95 percent / Et₃N / CH₂Cl₂ / 0 °C

With ammonium formate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1039/c39910000536

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 135253-85-9
Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / tetrabutylammonium hydrogen sulphate (TBAHS), 1 M aq. NaOH / CH₂Cl₂ / 25 °C

2: ammonium formate / 10percent Pd/C / methanol / 0.08 h / Heating

3: 95 percent / Et₃N / CH₂Cl₂ / 0 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; ammonium formate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1039/c39910000536