(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

Base Information

Chemical Name:(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester
CAS No.:148312-85-0
Molecular Formula:C₂₉H₃₀O₆
Molecular Weight:474.554
Hs Code.:

Synonyms:(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

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Chemical Property of (E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

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Technology Process of (E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

There total 7 articles about (E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl 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: 85.0%

: 148312-84-9
(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7,7-bis-ethylsulfanyl-hept-2-enoic acid methyl ester

: 148312-85-0
(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: With mercury dichloride; mercury(II) oxide; In water; acetone; for 5h; Heating;
DOI:10.1021/jo981211d

Reference yield:

: 116384-32-8
2,3,4-tri-O-benzyl-D-xylo-pentodialdose 1,1-diethyl dithioacetal

: 148312-85-0
(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 6 h / Ambient temperature

2: 85 percent / HgO, HgCl₂ / acetone; H₂O / 5 h / Heating

With mercury dichloride; mercury(II) oxide; In dichloromethane; water; acetone;
DOI:10.1021/jo981211d

Reference yield:

: 13263-74-6
D-xylose diethyl dithioacetal

: 148312-85-0
(E)-(4R,5S,6R)-4,5,6-Tris-benzyloxy-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 78 percent / imidazole / CH₂Cl₂ / 3 h

2: 1.) NaH, 2.) n-Bu₄N(+)*I(-) / 1) THF, rt, 1.5 h; 2) THF, rt, 8 h

3: 88 percent / n-Bu₄N(+)*F(-) / tetrahydrofuran / 2 h / Ambient temperature

4: 4-methylmorpholine N-oxide, 4 Angstroem molecular sieves, n-Pr₄N⁽¹⁺⁾*RuO₄^(1-) / CH₂Cl₂; acetonitrile / 0.83 h / Ambient temperature

5: CH₂Cl₂ / 6 h / Ambient temperature

6: 85 percent / HgO, HgCl₂ / acetone; H₂O / 5 h / Heating

With 1H-imidazole; tetrapropylammonium perruthennate; 4 A molecular sieve; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; 4-methylmorpholine N-oxide; mercury dichloride; mercury(II) oxide; In tetrahydrofuran; dichloromethane; water; acetone; acetonitrile;
DOI:10.1021/jo981211d