HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Toluenesulfonic acid → Oxiranemethanol, 3-[(phenylmethoxy)methyl]-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 2,2-Dimethoxypropane | HCID 6495 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Oxiranemethanol, 3-[(phenylmethoxy)methyl]- | HCID 3934498 | — |
Reaktionsschritte
2,2-Dimethoxypropane (12 mL, 97 mmol) was added with stirring to a solution of crude diols A and B, catalytic p-toluenesulfonic acid in acetone (50 mL). The mixture was stirred at room temperature overnight, diluted with ether and washed with aqueous sodium bicarbonate solution (twice). The organic extract was dried (magnesium sulfate), filtered and concentrated. The crude oil was chromatographed on a silica gel column and eluted with 2-10% ethyl acetate in hexanes to obtain dioxane C (5.85 g, 65% overall yield from 4-benzyloxy-2,3-epoxy-1-butanol) as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05827868 |
| Quelldatensatz | uspto-grants-1998_10 |
| ORD ID | ord-ede2c44152fa49799c2be5af1e02fafb |
| Quellennotiz | uspto-grants-1998_10 |