Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Nitrobenzene | HCID 7416 | — |
| Edukt | ((Chloromethyl)sulphonyl)benzene | HCID 81625 | — |
| Edukt | KOtBu THF | HCID 66863523 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Nitrobenzyl phenyl sulfone | HCID 363890 | 81% |
Reaktionsschritte
A solution of nitrobenzene (3.08 g, 25.0 mmol) and chloromethylphenylsulfone (4.76 g, 25.0 mmol) in dry THF is cooled to −50° C. and treated with 1.0M KOtBu/THF (55.0 mL, 55.0 mmol). The reaction is allowed to warm to −30° C. over 1 h, treated with glacial acetic acid (3.6 mL), warmed to 20° C., treated with water and extracted with CH2Cl2. The combined extracts are dried over MgSO4 and concentrated in vacuo. Chromatography (1:1 ethyl acetate:hexanes) of the resultant residue give the title product as a white solid, 5.62 g, (81% yield), mp 106-108° C., identified by mass spectral and HNMR analyses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07589108B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-c7c16c3a88de4ef6b69fba5c3cd2fb5f |
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| Quellennotiz | uspto-grants-2009_09 |
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