1-Bromo-3-chloropropane → 2-(3-Chloropropoxy)benzonitrile

HRID 1193658Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1193658
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9])#[N:2].Br[CH2:11][CH2:12][CH2:13][Cl:14].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O.C(Cl)(Cl)Cl>[Cl:14][CH2:13][CH2:12][CH2:11][O:9][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[C:1]#[N:2]

Komponenten

6

Edukt 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 119072-Hydroxybenzonitrile

Produkt 1

HCID 144071832-(3-Chloropropoxy)benzonitrileAusbeute 97,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 180AcetoneLösungsmittelHCID 6212ChloroformLösungsmittel

Versuchsvorschrift

A mixture of 2-cyanophenol (50.0 g, 0.42 mole), 1-bromo-3-chloropropane (67.7 g, 0.43 mole), and potassium carbonate (58.0 g, 0.42 mole) was heated overnight at gentle reflux in 500 ml of acetone. The reaction mixture was stripped to dryness and the residue was dissolved in chloroform. The chloroform layer was extracted several times with 5% sodium hydroxide. The chloroform layer was dried (anhydrous sodium sulfate), filtered, and the solvent was removed, to give a brown oil (80.09 g). A ten gram portion of this oil was subjected to flash chromatography on silica gel with 10% ethyl acetate-hexanes and 20% ethyl acetate-hexanes used for elution. Fractions were combined and solvent removed in vacuo. The clear oil obtained was dried 18 hrs in vacuo at room temperature and 8 hrs at 80° C. in vacuo. This furnished 5.24 g (50.0% yield--based on aliquot taken) of clear oil.

Aufarbeitung

  1. temperaturewas heated overnight
  2. extractionThe chloroform layer was extracted several times with 5% sodium hydroxide
  3. dry with materialThe chloroform layer was dried (anhydrous sodium sulfate)
  4. filtrationfiltered
  5. customthe solvent was removed

Quellen und Nachweise

ORD-Eintrag
ord-154662ab9ba846e3aa17028a641998a7
Quelldatensatz
uspto-grants-1989_03
Patentnummer
US04810713

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