HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzyl Bromide → 3,5-Dibenzyloxyiodobenzene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | 5-Iodobenzene-1,3-diol | HCID 616755 | — |
| Produkt | 3,5-Dibenzyloxyiodobenzene | HCID 15389195 | 96% |
Reaktionsschritte
3,5-Dihydroxyphenyl iodide (Tex. J. Sci., 1977, 28, 253) was reacted with two equivalents of benzyl bromide using the procedure described in Example 3 to give 3,5-dibenzyloxyphenyl iodide (96%), as an oil. This was reacted with n-butyl-lithium using the procedure described in the portion of Example 24 which is concerned with the preparation of starting materials and the organometallic reagent so formed was reacted with tetrahydropyran-4-one using the procedure described in that Example. There was thus obtained 4-(3,5-dibenzyloxyphenyl)-4-hydroxytetrahydropyran (60%), as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05403859 |
| Quelldatensatz | uspto-grants-1995_04 |
| ORD ID | ord-229b6bb505cd4257b1d60e890a372cf4 |
| Quellennotiz | uspto-grants-1995_04 |