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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1653752Erstellt: 25. Oktober 2026

Benzyl Bromide → 3,5-Dibenzyloxyiodobenzene

https://huagongshe.com/reaction/1653752

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt5-Iodobenzene-1,3-diolHCID 616755—
Produkt3,5-DibenzyloxyiodobenzeneHCID 1538919596%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05403859
Quelldatensatzuspto-grants-1995_04
ORD IDord-229b6bb505cd4257b1d60e890a372cf4
Quellennotizuspto-grants-1995_04