(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

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Chemical Name:(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester
CAS No.:634578-85-1
Molecular Formula:C₂₉H₃₆O₉S
Molecular Weight:560.665
Hs Code.:

Synonyms:(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

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Chemical Property of (E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

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Technology Process of (E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

There total 5 articles about (E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl 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: 84.0%

: 634578-83-9
(E)-(4R,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

: 634578-85-1
(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

Guidance literature:: With chloro-trimethyl-silane; water; In acetonitrile; at 20 ℃; for 8h;
DOI:10.1016/j.tetlet.2003.09.034

Reference yield:

: 634578-78-2
(E)-(S)-5-Formyloxy-hex-2-enoic acid 2-(toluene-4-sulfonyl)-ethyl ester

: 634578-85-1
(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / HCl / dioxane; H₂O / 12 h / 20 °C

2: 88 percent / 2,4,6-trichlorobenzoyl chloride; Et₃N; DMAP / tetrahydrofuran; toluene / 12 h / 20 °C

3: 84 percent / TMSCl; H₂O / acetonitrile / 8 h / 20 °C

With hydrogenchloride; dmap; chloro-trimethyl-silane; 2,4,6-trichlorobenzoyl chloride; water; triethylamine; In tetrahydrofuran; 1,4-dioxane; water; toluene; acetonitrile;
DOI:10.1016/j.tetlet.2003.09.034

Reference yield:

: 634578-65-7
trans-(5S)-5-hydroxy-p-toluenesulfonylethyl-2-hexenoate

: 634578-85-1
(E)-(4R,5S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-hex-2-enoic acid (E)-(S)-1-methyl-4-[2-(toluene-4-sulfonyl)-ethoxycarbonyl]-but-3-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / 2,4,6-trichlorobenzoyl chloride; Et₃N; DMAP / tetrahydrofuran; toluene / 12 h / 20 °C

2: 84 percent / TMSCl; H₂O / acetonitrile / 8 h / 20 °C

With dmap; chloro-trimethyl-silane; 2,4,6-trichlorobenzoyl chloride; water; triethylamine; In tetrahydrofuran; toluene; acetonitrile;
DOI:10.1016/j.tetlet.2003.09.034