benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

Base Information

Chemical Name:benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester
CAS No.:263843-21-6
Molecular Formula:C₂₄H₂₆O₅S₃
Molecular Weight:490.665
Hs Code.:

Synonyms:benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

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Chemical Property of benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

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Technology Process of benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

There total 6 articles about benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl 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%

: 98-09-9
benzenesulfonyl chloride

: 207737-17-5
toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxy-5-methylphenyl) ester

: 263843-21-6
benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1021/jm990281p

Reference yield:

: 62559-08-4
4-tert-butyl-2-nitrotoluene

: 263843-21-6
benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: H₂ / Raney Ni / methanol / 15 h / 35 °C / 2689.24 Torr

2: aq. NaNO₂; aq. 15percent H₂SO₄ / 0.5 h / 70 °C

3: Br₂; NaBr / methanol / 0.5 h / 5 - 40 °C

4: 79 percent / dithiothreitol; 0.02M KH₂PO₄ / ethanol / 4 h / Heating

5: 91 percent / pyridine / CCl₄

6: 70 percent / Et₃N / CH₂Cl₂

With pyridine; potassium dihydrogenphosphate; hydrogen; bromine; triethylamine; sodium bromide; sodium nitrite; diothiothreitol; nickel; In methanol; tetrachloromethane; ethanol; dichloromethane; 1: Reduction / 2: Diazotization / 3: Substitution / 4: Hydrolysis / 5: Tosylation / 6: Sulfonylation;
DOI:10.1021/jm990281p

Reference yield:

: 5781-02-2
5-(tert-butyl)-2-methylphenol

: 263843-21-6
benzenesulfonic acid 5-tert-butyl-2-methyl-4-(toluene-4-sulfonylsulfanyl)-phenyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: Br₂; NaBr / methanol / 0.5 h / 5 - 40 °C

2: 79 percent / dithiothreitol; 0.02M KH₂PO₄ / ethanol / 4 h / Heating

3: 91 percent / pyridine / CCl₄

4: 70 percent / Et₃N / CH₂Cl₂

With pyridine; potassium dihydrogenphosphate; bromine; triethylamine; sodium bromide; diothiothreitol; In methanol; tetrachloromethane; ethanol; dichloromethane; 1: Substitution / 2: Hydrolysis / 3: Tosylation / 4: Sulfonylation;
DOI:10.1021/jm990281p