Water → (6-Fluoro-benzo[1,3]dioxol-5-yl)-acetonitrile

HRID 503239Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 503239
Cl[CH2:2][C:3]1[C:11]([F:12])=[CH:10][C:6]2[O:7][CH2:8][O:9][C:5]=2[CH:4]=1.[C-:13]#[N:14].[Na+].O>CS(C)=O>[F:12][C:11]1[C:3]([CH2:2][C:13]#[N:14])=[CH:4][C:5]2[O:9][CH2:8][O:7][C:6]=2[CH:10]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

A mixture of 5-chloromethyl-6-fluoro-benzo[1,3]dioxole (640 mg, 3.4 mmol) and NaCN (340 mg, 6.8 mmol) in DMSO (20 mL) was stirred at 30° C. for 1 h and then poured into water. The mixture was extracted with EtOAc (50 mL×3). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried over Na2SO4, and evaporated under reduced pressure to give the crude product, which was purified by column chromatography on silica gel (5-10% ethyl acetate/petroleum ether) to afford (6-fluoro-benzo[1,3]dioxol-5-yl)-acetonitrile (530 mg, 70%). 1H-NMR (300 MHz, CDCl3) δ 6.82 (d, J=4.8, 1H), 6.62 (d, J=5.4, 1H), 5.99 (s, 2H), 3.65 (s, 2H).

Aufarbeitung

  1. extractionThe mixture was extracted with EtOAc (50 mL×3)
  2. washThe combined organic layers were washed with water (50 mL) and brine (50 mL)
  3. dry with materialdried over Na2SO4
  4. customevaporated under reduced pressure
  5. customto give the crude product, which
  6. customwas purified by column chromatography on silica gel (5-10% ethyl acetate/petroleum ether)

Quellen und Nachweise

ORD-Eintrag
ord-1c72c2d20b3f4116952a3082e457110c
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07776905B2

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