Hydrochloric Acid → alpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile

HRID 35550

Reaktionsgleichung

Reaktionsgleichung von HRID 35550
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[O:11][CH3:12].[OH-].[Na+].[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23]#[N:24])=[CH:18][CH:17]=1.Cl>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.O1CCCC1>[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([CH:22]([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=2[O:11][CH3:12])[C:23]#[N:24])=[CH:18][CH:17]=1

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 705192-Chloro-5-nitroanisoleHCID 2415824-Chlorobenzyl cyanide

Produkt 1

HCID 23035215alpha-(4-Chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 66133Benzyl triethylammonium chlorideKatalysatorHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a stirred mixture of 68 parts of 1-chloro-2-methoxy-4-nitrobenzene, 230 parts of a sodium hydroxide solution 50%, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 360 parts of tetrahydrofuran is added dropwise, during a 5 minutes period, a solution of 43.2 parts of 4-chlorobenzeneacetonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring is continued for 4 hours at 60° C. The reaction mixture is poured into 2000 parts of crushed ice. The whole is acidified with concentrated hydrochloric acid. The layers are separated. The aqueous phase is extracted with dichloromethane. The combined extracts are dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding α-(4-chlorophenyl)-2-methoxy-4-nitrobenzeneacetonitrile.

Aufarbeitung

  1. additionis added dropwise, during a 5 minutes period
  2. additionThe reaction mixture is poured into 2000 parts of crushed ice
  3. customThe layers are separated
  4. extractionThe aqueous phase is extracted with dichloromethane
  5. customThe combined extracts are dried
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue is crystallized from 2,2'-oxybispropane
  9. filtrationThe product is filtered off
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-fff9ae469d1a457387a4a6f72779f1b8
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04767760

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