(1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol

Base Information

• Chemical Name: (1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol
• CAS No.: 236401-80-2
• Molecular Formula: C₂₀H₃₁IO₄
• Molecular Weight: 462.368

Synonyms:(1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol

Chemical Property of (1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol

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Technology Process of (1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol

There total 1 articles about (1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol 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:

(3S,4S,5R,6S,7R,8R)-1-iodo-8-(4-methoxybenzyloxy)-4,6-isopropylidenedioxy-3,5,7-trimethylnon-1-ene → (1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol (236401-80-2)

Guidance literature:

With camphor-10-sulfonic acid; In methanol; dichloromethane; at 20 ℃;

DOI:10.1021/ol990004c

Reference yield:

(1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol (236401-80-2) + (E)-3-iodoacrylic acid (6372-02-7) → (3E,5E,7S,8S,11E,13E,15S,16S)-8,16-bis[(1S,2S,3S,4R)-2-hydroxy-4-(4-methoxybenzyloxy)-1,3-dimethylpentyl]-7,15-dimethyl-1,9-dioxacyclohexadeca-3,5,11,13-tetraene-2,10-dione (236401-66-4) + (3E,5E,7S,8S,9R,10R,13E,15E,17S,18S,19R,20R,23E,25E,27S,28S,29R,30R)-10,20,30-tris[(1R,2R)-2-(4-methoxybenzyloxy)-1-methylpropyl]-7,9,17,19,27,29-hexamethyl-8,18,28-trihydroxy-1,11,21-trioxacyclotriaconta-3,5,13,15,23,25-hexaene-2,12,22-trione

Guidance literature:

Multistep reaction.;

DOI:10.1021/ol990004c

Reference yield:

(1E,3S,4S,5R,6S,7S,8R)-1-iodo-8-(4-methoxybenzyloxy)-3,5,7-trimethylnon-1-en-4,6-diol (236401-80-2) + (E)-3-iodoacrylic acid (6372-02-7) → (3E,5E,7S,8S,11E,13E,15S,16S)-8,16-bis[(1S,2S,3S,4R)-2-hydroxy-4-(4-methoxybenzyloxy)-1,3-dimethylpentyl]-7,15-dimethyl-1,9-dioxacyclohexadeca-3,5,11,13-tetraene-2,10-dione (236401-66-4) + (3E,5E,7S,8S,9R,10R,13E,15E,17S,18S,19R,20R,23E,25E,27S,28S,29R,30R)-10,20,30-tris[(1R,2R)-2-(4-methoxybenzyloxy)-1-methylpropyl]-7,9,17,19,27,29-hexamethyl-8,18,28-trihydroxy-1,11,21-trioxacyclotriaconta-3,5,13,15,23,25-hexaene-2,12,22-trione + (3E,5E,7S,8S,11E,13E,15S,16S,19E,21E,23S,24S)-8,16,24-tris[(1S,2S,3S,4R)-2-hydroxy-4-(4-methoxybenzyloxy)-1,3-dimethylpentyl]-7,15,23-trimethyl-1,9,17-tri-trioxacyclotetracosa-3,5,11,13,19,21-hexaene-2,10,18-trione

Guidance literature:

Multistep reaction.;

DOI:10.1021/ol990004c

Downstream raw materials:

(3E,5E,7S,8S,11E,13E,15S,16S)-8,16-bis[(1S,2S,3S,4R)-2-hydroxy-4-(4-methoxybenzyloxy)-1,3-dimethylpentyl]-7,15-dimethyl-1,9-dioxacyclohexadeca-3,5,11,13-tetraene-2,10-dione

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