2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

Base Information

Chemical Name:2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester
CAS No.:181624-34-0
Molecular Formula:C₇₈H₉₀O₉
Molecular Weight:1171.57
Hs Code.:

2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

Synonyms:2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

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Chemical Property of 2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

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Technology Process of 2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

There total 8 articles about 2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl 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:

: 5350-57-2
benzophenone hydrazone

: 181624-34-0
2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 3 steps

1: HgO

2: K₂CO₃ / acetone

3: 18 percent / NIS, TFOH / CH₂Cl₂; ethyl acetate / 1 h / -40 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; potassium carbonate; mercury(II) oxide; In dichloromethane; ethyl acetate; acetone;
DOI:10.7164/antibiotics.49.713

Reference yield:

: 4132-28-9,4291-69-4,6386-24-9,6564-72-3,59531-24-7,69257-52-9,78184-89-1,78609-16-2,78609-17-3,78609-18-4,96553-53-6,104111-61-7,131347-08-5
2,3,4,6-tetra-O-benzyl-D-mannopyranose

: 181624-34-0
2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent

2: 18 percent / NIS, TFOH / CH₂Cl₂; ethyl acetate / 1 h / -40 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; ethyl acetate;
DOI:10.7164/antibiotics.49.713

Reference yield:

: 73274-87-0,73713-38-9
3-hydroxy-7-methoxy-3H-isobenzofuran-1-one

: 181624-34-0
2-Benzyloxy-6-[(R)-16-((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-heptadecyl]-benzoic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 5 steps

2: 87 percent / LiCl / dimethylformamide / 3 h / 150 °C

3: HgO

4: K₂CO₃ / acetone

5: 18 percent / NIS, TFOH / CH₂Cl₂; ethyl acetate / 1 h / -40 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; potassium carbonate; lithium chloride; mercury(II) oxide; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.7164/antibiotics.49.713