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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530276Erstellt: 25. Oktober 2026

Dibenzyl ether → 6-Benzyloxyhexanal

https://huagongshe.com/reaction/530276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibenzyl etherHCID 7657—
Edukt2-[2-(Carboxylatomethyl)-3-iodophenyl]acetateHCID 21945688—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-BenzyloxyhexanalHCID 389877—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of alcohol (22, 6-(benzyloxy)hexan-1-01) dissolved in dry DCM, Tempo free radical (0.1 equiv), iodobenzenediacetate (1.1 equiv) were added and stirred at 25° C. On completion of the reaction (by checking TLC), it was quenched with dilute solution of Na2S2O3. The organic layer was extracted in DCM, washed with brine, dried over anhydrous Na2SO4. The solvent was removed in vacuum concentrated and subjected for chromatographic separation. The eluent was allowed to come in a solution of pet ether:EtOAC=95:5 as a colorless liquid. 1H NMR (CDCl3, 200 MHz): δ 9.8 (s, 1H), 7.2-7.4 (m, 5H), 4.5 (s, 2H), 3.5 (t, 2H), 2.4 (t, 2H), 1.6 (m, 4H), 1.4 (m, 4H); 13C NMR (CDCl3, 50 MHz): δ 202.75, 138.50, 128.40, 127.68, 127.50, 72.95, 70.03, 43.86, 29.53, 25.85, 21.91.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09353077B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-47158f6f297144b6982820657352f70b
Quellennotizuspto-grants-2016_05