Reaktion #1563901

ord-e494f6738b9e4660aa2deb545f788bb1

Reaktionsgleichung

OCc1ccc2c(c1)OCO2
3,4-(methylenedioxy)benzyl alcohol
II
I2
OCc1cc2c(cc1I)OCO2
(6-iodobenzo[d][1,3]dioxol-5-yl)methanol
Ausbeute 56.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
-5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered
  2. 2
    WaschenThe filtrate was washed with 20% Na2S2O3
  3. 3
    Sonstigedried
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe crude was purified by column chromatography on silica gel (petroleum ether)

Vorschrift

To a solution of 3,4-(methylenedioxy)benzyl alcohol (1.8 g, 12 mmol) and CF3COOAg (3.434 g, 15.5 mmol) in dry CHCl3 (55 mL) at −5° C. was added I2 (3.9 g, 15.5 mmol) in portion. The resulting yellow mixture was maintain at −5° C. for 5 min, then filtered. The filtrate was washed with 20% Na2S2O3, dried and evaporated. The crude was purified by column chromatography on silica gel (petroleum ether) to obtain (6-iodobenzo[d][1,3]dioxol-5-yl)methanol (1.8 g, 56%) as a white solid. LCMS: 279[M+1]+; 1H NMR (DMSO-d6) δ 4.31 (d, 2H, J=4.2 Hz), 5.40 (t, 1H, J=4.2 Hz), 6.03 (s, 2H), 7.03 (s, 1H), 7.34 (s, 2H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09402832B2uspto-grants-2016_08