(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester
CAS No.:143332-45-0
Molecular Formula:C₄₁H₄₀Cl₃NO₁₆
Molecular Weight:909.125
Hs Code.:

(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Synonyms:(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

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Chemical Property of (2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

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Technology Process of (2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

There total 5 articles about (2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic 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:

: 98-88-4
benzoyl chloride

: 143332-45-0
(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / pyridine

3: 72 percent / TMSOTf / CH₂Cl₂ / 1 h / -20 °C

4: H₂ / 10percent Pd-C / ethyl acetate / 3 h / Ambient temperature

5: K₂CO₃ / CH₂Cl₂ / 4 h / Ambient temperature

With pyridine; trimethylsilyl trifluoromethanesulfonate; hydrogen; potassium carbonate; palladium on activated charcoal; In dichloromethane; ethyl acetate;

Reference yield:

: 105285-86-7
benzyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside

: 143332-45-0
(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

2: 72 percent / TMSOTf / CH₂Cl₂ / 1 h / -20 °C

3: H₂ / 10percent Pd-C / ethyl acetate / 3 h / Ambient temperature

4: K₂CO₃ / CH₂Cl₂ / 4 h / Ambient temperature

With trimethylsilyl trifluoromethanesulfonate; hydrogen; potassium carbonate; palladium on activated charcoal; In dichloromethane; ethyl acetate;

Reference yield:

: 143332-41-6
Benzoic acid (2S,3R,4R,5R,6R)-5-acetoxy-6-benzyloxy-4-hydroxy-2-methyl-tetrahydro-pyran-3-yl ester

: 143332-45-0
(2S,4aR,6S,7R,8S,8aR)-6-[(2S,3R,4R,5S,6S)-3-Acetoxy-5-benzoyloxy-6-methyl-2-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yloxy]-7,8-bis-benzoyloxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / TMSOTf / CH₂Cl₂ / 1 h / -20 °C

2: H₂ / 10percent Pd-C / ethyl acetate / 3 h / Ambient temperature

3: K₂CO₃ / CH₂Cl₂ / 4 h / Ambient temperature

With trimethylsilyl trifluoromethanesulfonate; hydrogen; potassium carbonate; palladium on activated charcoal; In dichloromethane; ethyl acetate;