Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dibenzyl ether | HCID 7657 | — |
| Edukt | 2-[2-(Carboxylatomethyl)-3-iodophenyl]acetate | HCID 21945688 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 6-Benzyloxyhexanal | HCID 389877 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09353077B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-47158f6f297144b6982820657352f70b |
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| Quellennotiz | uspto-grants-2016_05 |
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