Reaktion #7835

ord-768846e0a8dc4bde93680feebe296211

Reaktionsgleichung

O=C(O)c1ccc(CBr)c(Cl)c1
4-(bromomethyl)-3-chlorobenzoic acid
[C-]#N.[Na+]
NaCN
Cl
HCl
N#CCc1ccc(C(=O)Cl)cc1Cl
3-chloro-4-(cyanomethyl)benzoyl chloride

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled to rt
  2. 2
    ExtraktionThe aqueous mixture was extracted with CH2Cl2 (3×25 mL)
  3. 3
    EinengenThe combined organic layers were concentrated under reduced pressure
  4. 4
    workup.DISSOLUTIONdissolved in MTBE
  5. 5
    WaschenThe organic mixture was washed with H2O and brine (3×25 mL)
  6. 6
    Trocknendried over MgSO4
  7. 7
    Filtrationfiltered
  8. 8
    Einengenconcentrated

Vorschrift

A suspension of 4-(bromomethyl)-3-chlorobenzoic acid (4.0 g, 16 mmol) in DMF (120 mL) and H2O (40 mL) was treated with NaCN (2.4 g, 49 mmol) and heated to 80° C. for 2 h. The mixture was cooled to rt and acidified with 1N HCl. The aqueous mixture was extracted with CH2Cl2 (3×25 mL). The combined organic layers were concentrated under reduced pressure and dissolved in MTBE. The organic mixture was washed with H2O and brine (3×25 mL), dried over MgSO4, filtered and concentrated to afford 3-chloro-4-(cyanomethyl)benzoyl chloride.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08