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Bromine → 3'-(2-Bromoacetyl)-4'-fluoromethanesulfonanilide

HRID 2379183
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2379183
[C:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[F:15])[NH:7][S:8]([CH3:11])(=[O:10])=[O:9])(=[O:3])[CH3:2].[Br:16]Br>C(O)(=O)C>[Br:16][CH2:2][C:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[F:15])[NH:7][S:8]([CH3:11])(=[O:10])=[O:9])=[O:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24408BromineHCID 111071753'-Acetyl-4'-fluoromethanesulfonanilide

Produkt 1

HCID 221413933'-(2-Bromoacetyl)-4'-fluoromethanesulfonanilideAusbeute 88,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

3'-Acetyl-4'-fluoromethanesulfonanilide (32 g) was dissolved in 250 ml of acetic acid, then 22.1 g of bromine was dropped thereinto gradually at room temperature and the mixture was made to react at room temperature for 3 hours. The reaction mixture was added to ice water and the mixture-was extracted with ethyl acetate. The extract was washed with aqueous solution of sodium bicarbonate, then with water, dried and the solvent was evaporated therefrom followed by crystallizing from diisopropyl ether to give 38 g of 3'-(2-bromoacetyl)-4'-fluoromethanesulfonanilide, m.p. 110°-113° C.

Aufarbeitung

  1. customgradually at room temperature
  2. customto react at room temperature for 3 hours
  3. extractionthe mixture-was extracted with ethyl acetate
  4. washThe extract was washed with aqueous solution of sodium bicarbonate
  5. dry with materialwith water, dried
  6. customthe solvent was evaporated
  7. customby crystallizing from diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-7bc91113b29840a0856437345ad235fd
Quelldatensatz
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05360822

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