HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → Toluene 4-thiosulfonic acid S-[2-tert-butyl-4-(2-methoxymethoxy-ethoxy)-5-methyl-phenyl] ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Methylbenzene-1-sulfonyl bromide | HCID 10130885 | — |
| Edukt | 2-Tert-butyl-4-(2-methoxymethoxy-ethoxy)-5-methyl-benzenethiol | HCID 18798700 | — |
| Lösungsmittel | 1,1,2-Trichloroethane | HCID 6574 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Toluene 4-thiosulfonic acid S-[2-tert-butyl-4-(2-methoxymethoxy-ethoxy)-5-methyl-phenyl] ester | HCID 53987067 | — |
Reaktionsschritte
A solution of tosyl bromide (21.0 g; 89.32 mmol), 50 mL of trichloroethane and 20 mL of NEt3 was cooled to 0° C. To this solution was added slowly a solution of 12.4 mmol of 2-tert-butyl-4-(2-methoxymethoxy-ethoxy)-5-methyl-benzenethiol (prepared in Example AAAA) in 100 mL of trichloroethane. After 13 hours, the reaction mixture was diluted with EtOAc and washed with brine. The product was purified by flash silica gel chromatography, eluting with EtOAc:hexane (5:95, then switching to 3:7).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05834506 |
| Quelldatensatz | uspto-grants-1998_11 |
| ORD ID | ord-295045b58ba843feb787f80e37f1aa1e |
| Quellennotiz | uspto-grants-1998_11 |