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Bromine → 2-(3',5'-Dichlorophenyl)-4,4-dimethyl-5-bromomethylenoxazoline hydrobromide

HRID 1780003
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1780003
[CH3:1][C:2]([NH:6][C:7](=[O:16])[C:8]1[CH:13]=[C:12]([Cl:14])[CH:11]=[C:10]([Cl:15])[CH:9]=1)([CH3:5])[C:3]#[CH:4].[Br:17]Br>C(Cl)Cl.CCCCCC>[BrH:17].[Cl:14][C:12]1[CH:13]=[C:8]([C:7]2[O:16][C:3](=[CH:4][Br:17])[C:2]([CH3:1])([CH3:5])[N:6]=2)[CH:9]=[C:10]([Cl:15])[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 24408Bromine2×HCID 32154Propyzamide

Produkt 1

HCID 677267812-(3',5'-Dichlorophenyl)-4,4-dimethyl-5-bromomethylenoxazoline hydrobromideAusbeute 178,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittel2×HCID 8058HexaneLösungsmittel

Versuchsvorschrift

N- (1',1'-dimethylpropynyl)-3,5-dichlorobenzamide (40 gm, 0.156 m) was dissolved in methylene chloride (600 ml) and bromine (25 gm, 0.156 m) in methylene chloride (100 ml) was added gradually with stirring at room temperature. After the complete addition of the bromine, the mixture was stirred for another 15 minutes and diluted with hexane (500 ml). The yellowish-white precipitate which formed was filtered and dried to yield 58 gm of 2-(3',5'-dichlorophenyl)-4,4-dimethyl-5-bromomethylenoxazoline hydrobromide. The oxazoline hydrobromide (55 gm, 0.13 m) was added to concentrated sulfuric acid (200 ml) and stirred to obtain a clear solution. Water (20 ml) was added and the mixture heated at about 50° C. for about 24 hours. The mixture was then poured into ice water (about 2000 ml) and the white precipitate which formed was filtered and dried. Recrystallization from isopropanol, ether and hexane (1:1:2) yielded 21 gm of pure product.

Aufarbeitung

  1. stirringthe mixture was stirred for another 15 minutes
  2. customThe yellowish-white precipitate which formed
  3. filtrationwas filtered
  4. customdried

Quellen und Nachweise

ORD-Eintrag
ord-d018dcc9ccaf4c66914144264432016f
Quelldatensatz
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05629346

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