Reaktion #1730850

Reaktionsgleichung

4-allyl-3,5-bis-benzyloxy-benzoic acid tert-butyl ester

m-CPBA

→

title compound

Ausbeute 57.9%

3,5-Bis-benzyloxy-4-oxiranylmethyl-benzoic acid tert-butyl ester

Ausbeute 57.9%

Lösungsmittel

CH2Cl2

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe mixture was refluxed overnight
2. 2
   FiltrationThe solid was filtered
3. 3
   Waschenwashed with CH2Cl2
4. 4
   WaschenThe combined filtrates were washed with saturated aqueous Na2S2O4 (250 mL) and brine (250 mL)
5. 5
   TrocknenThe organic layer was dried over Na2SO4
6. 6
   Einengenconcentrated
7. 7
   Sonstigeto give a yellow oil
8. 8
   SonstigeThe crude oil was purified by flash column chromatography (EtOAc/petroleum ether=1/20)

Vorschrift

To a solution of 4-allyl-3,5-bis-benzyloxy-benzoic acid tert-butyl ester (200d) (125 g, 0.29 mol) in CH2Cl2 was added m-CPBA (100 g, 0.58 mol) in several portions. The mixture was refluxed overnight. The solid was filtered and washed with CH2Cl2. The combined filtrates were washed with saturated aqueous Na2S2O4 (250 mL) and brine (250 mL). The organic layer was dried over Na2SO4 and concentrated to give a yellow oil. The crude oil was purified by flash column chromatography (EtOAc/petroleum ether=1/20) to give the title compound (75 g, 57.8%) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.40 (m, 12H), 5.09(s, 4H), 3.53 (dd, 1H), 3.17 (m, 1H), 2.80 (dd, H), 2.63 (t, 1H), 2.51 (dd, 1H), 1.60 (s, 9H).

Quelle