Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

Base Information

Chemical Name:Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester
CAS No.:139526-01-5
Molecular Formula:C₃₂H₃₁NO₁₀
Molecular Weight:589.599
Hs Code.:

Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

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Chemical Property of Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

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Technology Process of Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

There total 5 articles about Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-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:

: 138906-43-1
4-methoxyphenyl 4,6-di-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 139526-01-5
Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / NEt₃ / 1,2-dichloro-ethane / 5 h / Ambient temperature

2: 78 percent / BH₃*Me₃N, AlCl₃, molecular sieve 4A / tetrahydrofuran / Ambient temperature

3: 81 percent / Et₂NSF₃ / tetrahydrofuran / 50 °C

4: 95 percent / 1M NaOMe / methanol; CH₂Cl₂ / 0 °C

5: pyridine, 4-dimethylaminopyridine / Ambient temperature

With pyridine; dmap; aluminium trichloride; diethylamino-sulfur trifluoride; trimethylamine-borane; 4 A molecular sieve; sodium methylate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jo00032a601

Reference yield:

: 139525-98-7
p-methoxyphenyl 6-O-benzyl-3,4-O-carbonyl-2-deoxy-2-phthalimido-β-D-galactopyranoside

: 139526-01-5
Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 1M NaOMe / methanol; CH₂Cl₂ / 0 °C

2: pyridine, 4-dimethylaminopyridine / Ambient temperature

With pyridine; dmap; sodium methylate; In methanol; dichloromethane;
DOI:10.1021/jo00032a601

Reference yield:

: 139525-96-5
p-methoxyphenyl 6-O-benzyl-2-deoxy-3-O-(phenylcarbamoyl)-2-phthalimido-β-D-glucopyranoside

: 139526-01-5
Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / Et₂NSF₃ / tetrahydrofuran / 50 °C

2: 95 percent / 1M NaOMe / methanol; CH₂Cl₂ / 0 °C

3: pyridine, 4-dimethylaminopyridine / Ambient temperature

With pyridine; dmap; diethylamino-sulfur trifluoride; sodium methylate; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jo00032a601