Acetic Acid → (Pyren-1-ylmethylene)malononitrile

HRID 1112341

Reaktionsgleichung

Reaktionsgleichung von HRID 1112341
[C:1]1([CH:17]=O)[C:14]2[C:15]3=[C:16]4[C:11](=[CH:12][CH:13]=2)[CH:10]=[CH:9][CH:8]=[C:7]4[CH:6]=[CH:5][C:4]3=[CH:3][CH:2]=1.[C:19](#[N:23])[CH2:20][C:21]#[N:22].C(O)(=O)C.C([O-])(=O)C.[NH4+]>O1CCCC1.C(O)C.ClC1C=CC=CC=1.C1C=CC=CC=1>[C:21]([C:20]([C:19]#[N:23])=[CH:17][C:1]1[C:14]2[C:15]3=[C:16]4[C:11](=[CH:12][CH:13]=2)[CH:10]=[CH:9][CH:8]=[C:7]4[CH:6]=[CH:5][C:4]3=[CH:3][CH:2]=1)#[N:22]

Komponenten

9

Edukt 4

HCID 176Acetic AcidHCID 8010MalononitrileHCID 2328481-PyrenecarboxaldehydeHCID 517165Ammonium Acetate

Produkt 1

HCID 290168(Pyren-1-ylmethylene)malononitrile

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 241BenzeneLösungsmittelHCID 702EthanolLösungsmittelHCID 7964ChlorobenzeneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

About 100 grams (0.434 moles) pyrene-1-carboxaldehyde, about 28.7 grams (0.434 moles) malononitrile, about 10.4 milliliters acetic acid, about 3.48 grams ammonium acetate and about 400 milliliters benzene are heated to boiling under reflux conditions for 30 minutes. The entire contents of the flask crystallized, forming a deep orange red product which is soluble in tetrahydrofuran, moderately soluble in ethanol and very soluble in chlorobenzene. This product is recrystallized from a mixture of chlorobenzene and ethanol (30:70). Yield: 104.4 grams m. p 248°-250° C.

Aufarbeitung

  1. customThe entire contents of the flask crystallized
  2. customforming a deep orange red product which
  3. customThis product is recrystallized from a mixture of chlorobenzene and ethanol (30:70)
  4. customp 248°-250° C.

Quellen und Nachweise

ORD-Eintrag
ord-9c9ed8e113d747768ff0cc87f7818130
Quelldatensatz
uspto-grants-1978_10
Patentnummer
US04122114

Verknüpfte Notizen

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