((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

Base Information

Chemical Name:((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid
CAS No.:557087-94-2
Molecular Formula:C₃₀H₃₄O₇
Molecular Weight:506.596
Hs Code.:

Synonyms:((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

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Chemical Property of ((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

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Technology Process of ((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

There total 8 articles about ((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid 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: 97.0%

: 557088-28-5
methyl (4R)-2,3,6-tri-O-benzyl-4-deoxy-4-(2-ethanal)-α-D-glucopyranoside

: 557087-94-2
((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

Guidance literature:: With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; In water; tert-butyl alcohol; at 20 ℃; for 1h;
DOI:10.1021/jo030039x

Reference yield:

: 138607-78-0
3,4-dibenzyloxy-2-methoxy-3,4,8,8a-tetrahydro-2H-pyrano[3,4-b]pyran-6-one

: 557087-94-2
((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / Pd / C / ethanol

2: LiOH / tetrahydrofuran; H₂O / 0.08 h

3: 1) NaH / 2) n-Bu₄NI / 1) THF, DMF, 2) overnight

With lithium hydroxide; hydrogen; sodium hydride; palladium on activated charcoal; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; ethanol; water;
DOI:10.1021/jo00028a017

Reference yield:

: [(2S,4S,5R,6S)-4,5-Bis-benzyloxy-6-methoxy-2-(4-methoxy-benzyloxymethyl)-dihydro-pyran-(3Z)-ylidene]-acetic acid methyl ester

: 557087-94-2
((2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / ceric ammonium nitrate (CAN) / acetonitrile; H₂O / 3 h / 0 °C

2: H₂ / Pd / C / ethanol

3: LiOH / tetrahydrofuran; H₂O / 0.08 h

4: 1) NaH / 2) n-Bu₄NI / 1) THF, DMF, 2) overnight

With lithium hydroxide; ammonium cerium(IV) nitrate; hydrogen; sodium hydride; palladium on activated charcoal; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; ethanol; water; acetonitrile;
DOI:10.1021/jo00028a017