Reaktion #6943

ord-d5067be8faaa479d8cc0710e9fd56529

Reaktionsgleichung

CI
MeI
Cc1ccc(C(=O)CC#N)cc1
3-(4-Methyl-phenyl)-3-oxo-propionitrile
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(=O)CCl
1-chloro-propan-2-one
S=C=S
CS2
CSc1sc(C(C)=O)c(-c2ccc(C)cc2)c1C#N
desired product
CSc1sc(C(C)=O)c(-c2ccc(C)cc2)c1C#N
5-Acetyl-2-methylsulfanyl-4-(4-methyl-phenyl)-thiophene-3-carbonitrile

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe resulting mixture stirred at room temperature for an additional 10 minutes
  2. 2
    workup.WAITAfter 1 hour
  3. 3
    workup.WAITAfter 30 minutes
  4. 4
    workup.ADDITIONthe mixture was poured onto water
  5. 5
    workup.STIRRINGthe resulting mixture was stirred vigorously for 12–16 hours
  6. 6
    Sonstigeto afford

Vorschrift

3-(4-Methyl-phenyl)-3-oxo-propionitrile (5 mmol) was added to a suspension of K2CO3 (3 equivalents, 15 mmol) in DMF (4.5 mL) and allowed to stir at room temperature. After 10 minutes, CS2 (1.25 equivalents, 7.5 mmol) was added in one portion and the resulting mixture stirred at room temperature for an additional 10 minutes. A solution of 1-chloro-propan-2-one (1.0 equivalent, 5 mmol) in DMF (5 mL) was added. After 1 hour, a solution of MeI (1.1 equivalents, 5.5 mmol) in DMF (2 mL) was added in a dropwise fashion. After 30 minutes, the mixture was poured onto water and the resulting mixture was stirred vigorously for 12–16 hours to afford a suspension of the desired product. The crude product was isolated by filtration.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084159B2uspto-grants-2006_08