2-(Allyloxy)-5-bromobenzaldehyde → 5-Bromo-2-(2-propen-1-yloxy)benzenemethanol

HRID 1870752Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1870752
[CH2:1]([O:4][C:5]1[CH:12]=[CH:11][C:10]([Br:13])=[CH:9][C:6]=1[CH:7]=[O:8])[CH:2]=[CH2:3].[BH4-].[Na+]>O>[CH2:1]([O:4][C:5]1[CH:12]=[CH:11][C:10]([Br:13])=[CH:9][C:6]=1[CH2:7][OH:8])[CH:2]=[CH2:3]

Komponenten

4

Edukt 2

HCID 21687062-(Allyloxy)-5-bromobenzaldehydeHCID 4311764Sodium borohydride

Produkt 1

HCID 21940165-Bromo-2-(2-propen-1-yloxy)benzenemethanolAusbeute 96,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A solution of 2-allyloxy-5-bromobenzaldehyde (5.27 g, 21.9 mM) was treated with sodium borohydride, (0.415 g, 10.9 mM). The reaction was stirred at ambient temperature for 21/2 hours, water was added and the solvent removed at reduced pressure. The residue was acidified to pH 1 and extracted with ethyl acetate twice. The organic layers were combined, dried (MgSO4) and evaporated to give 2-allyloxy-5-bromobenzyl alcohol (5.12 g, 96%) as a white solid.

Aufarbeitung

  1. additionwas added
  2. customthe solvent removed at reduced pressure
  3. extractionextracted with ethyl acetate twice
  4. dry with materialdried (MgSO4)
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-edc9e29f340046679bfad0cf545cd2e2
Quelldatensatz
uspto-grants-2000_08
Patentnummer
US06100258

Notizen zur Reaktion

Wird geladen…