Bromine → 3-Bromo-5-chlorobenzo[b]thiophene

HRID 278002Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 278002
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[CH:7][C:6]=2[CH:10]=1.[Br:11]Br>C(O)(=O)C>[Br:11][C:7]1[C:6]2[CH:10]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[S:9][CH:8]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a solution of 0.30 gm (1.77 mMol) 5-chlorobenzothiophene 1.0 mL acetic acid was added a solution of 0.31 gm (1.95 mMol) bromine in 1.0 mL acetic acid under a nitrogen atmosphere. The reaction was heated to 50° C. for 4 hours at which time the volatiles were removed under reduced pressure. The residue was partitioned between dichloromethane and aqueous sodium bicarbonate. The phases were separated and the organics were washed with saturated aqueous sodium chloride, dried over sodium sulfate and concentrated under reduced pressure to give 0.335 gm (76%) of the title compound as a tan solid. m.p.=85-86° C. MS(FD): m/e=249 (M+2).

Aufarbeitung

  1. customwere removed under reduced pressure
  2. customThe residue was partitioned between dichloromethane and aqueous sodium bicarbonate
  3. customThe phases were separated
  4. washthe organics were washed with saturated aqueous sodium chloride
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-fcfc6b28db2c4c00aa565a407012d32d
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06358972B1

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