Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

Base Information

Chemical Name:Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester
CAS No.:211801-80-8
Molecular Formula:C₃₄H₄₇NO₈S₂
Molecular Weight:661.881
Hs Code.:

Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

Synonyms:Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

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Chemical Property of Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

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Technology Process of Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

There total 4 articles about Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl 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: 70.0%

: 98-59-9
p-toluenesulfonyl chloride

: 201136-64-3
(E)-(4S,7R,8S,9S,16S)-4,8-Dihydroxy-13-hydroxymethyl-5,5,7,9-tetramethyl-16-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-oxacyclohexadec-13-ene-2,6-dione

: 211801-80-8
Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1016/S0040-4020(98)00352-4

Reference yield:

: 201136-77-8
(12E,16E)-(3S,6R,7S,8S,15S)-3,7-Bis-(tert-butyl-dimethyl-silanyloxy)-15-hydroxy-4,4,6,8,16-pentamethyl-17-(2-methyl-thiazol-4-yl)-5-oxo-12-trityloxymethyl-heptadeca-12,16-dienoic acid

: 211801-80-8
Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Et₃N, 2,4,6-trichlorobenzoyl chloride, 2.) 4-dimethylaminopyridine / 1.) THF, 0 deg C, 1 h, 2.) THF, toluene, 75 deg C, 3 h

2: 78 percent / HF*pyridine / tetrahydrofuran / 24 h / Ambient temperature

3: 70 percent / Et₃N, 4-dimethylaminopyridine / CH₂Cl₂ / 1 h / 0 °C

With dmap; 2,4,6-trichlorobenzoyl chloride; pyridine hydrogenfluoride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)00352-4

Reference yield:

: 201136-78-9
(E)-(4S,7R,8S,9S,16S)-4-(tert-Butyl-dimethyl-silanyloxy)-8-hydroxy-5,5,7,9-tetramethyl-16-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-13-trityloxymethyl-oxacyclohexadec-13-ene-2,6-dione

: 211801-80-8
Toluene-4-sulfonic acid (E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-2-[(E)-1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-12,16-dioxo-oxacyclohexadec-4-en-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / 30percent HF*pyridine / tetrahydrofuran / 24 h / 0 - 25 °C

2: Et₃N, DMAP / CH₂Cl₂ / 1 h / 0 °C

With dmap; pyridine hydrogenfluoride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1039/a705845d