Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

Base Information

Chemical Name:Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester
CAS No.:666739-71-5
Molecular Formula:C₃₄H₄₂F₃NO₈S₂
Molecular Weight:713.837
Hs Code.:

Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

Synonyms:Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

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Chemical Property of Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

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Technology Process of Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

There total 18 articles about Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-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: 35.0%

: 98-59-9
p-toluenesulfonyl chloride

: 666739-59-9
F₃-deH-dEpoF

: (10E,13E)-(4S,7R,8S,9S,16S)-16-[(E)-2-(2-Chloromethyl-thiazol-4-yl)-1-methyl-vinyl]-4,8-dihydroxy-5,5,7,9-tetramethyl-13-trifluoromethyl-oxacyclohexadeca-10,13-diene-2,6-dione

: 666739-71-5
Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 1.5h;
DOI:10.1021/ja046992g

Reference yield:

: 503818-19-7
(3S,6R,7S,8S)-7-(tert-Butyl-dimethyl-silanyloxy)-4,4,6,8-tetramethyl-5-oxo-3-triethylsilanyloxy-dec-9-enoic acid

: 666739-71-5
Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: EDCI; DMAP / CH₂Cl₂ / 0 - 20 °C

2: 78 percent / second generation Grubbs' catalyst / toluene / 110 °C

3: t-BuOK / tetrahydrofuran / -78 - -20 °C

4: 54 percent / HF*pyridine / tetrahydrofuran / 20 °C

5: 35 percent / Et₃N; DMAP / CH₂Cl₂ / 1.5 h / 20 °C

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; dmap; potassium tert-butylate; pyridine hydrogenfluoride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/ja046992g

Reference yield:

: 637003-66-8
(E)-(S)-3-Hydroxy-6-trifluoromethyl-nona-5,8-dien-2-one

: 666739-71-5
Toluene-4-sulfonic acid 4-[(E)-2-((4E,7E)-(2S,9S,10S,11R,14S)-10,14-dihydroxy-9,11,13,13-tetramethyl-12,16-dioxo-5-trifluoromethyl-oxacyclohexadeca-4,7-dien-2-yl)-propenyl]-thiazol-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 4.85 g / EDCI; DMAP / CH₂Cl₂ / 0 - 20 °C

2.1: 76 percent / second generation Grubbs' catalyst / toluene / 0.28 h / 110 °C

3.1: t-BuOK / tetrahydrofuran / 0.33 h / 0 °C

3.2: 74 percent / tetrahydrofuran / 2 h / -78 - 20 °C

4.1: 96 percent / HF*pyridine / tetrahydrofuran / 4.3 h / 20 °C

5.1: 35 percent / Et₃N; DMAP / CH₂Cl₂ / 1.5 h / 20 °C

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; dmap; potassium tert-butylate; pyridine hydrogenfluoride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; toluene; 3.2: Wittig reaction;
DOI:10.1021/ja046992g