Hydrochloric Acid → 5-(2-Bromophenyl)-4-pentynoic acid

HRID 1722333Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1722333
[C:1]([OH:7])(=[O:6])[CH2:2][CH2:3][C:4]#[CH:5].[Br:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1I.Cl>C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Pd].[Cu]I.C(NCC)C>[Br:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:5]#[C:4][CH2:3][CH2:2][C:1]([OH:7])=[O:6]

Komponenten

7

Versuchsvorschrift

To 10 ml of diethylamine was added with stirring 0.5 g (5.1 mmol) of 4-pentynoic acid, 1.4g (5 mmol) of 1-bromo-2-iodobenzene, and 60mg (0.05 mmol) of tetrakis(triphenylphosphine)palladium(O) The slurry was degassed with argon and 0.19g (1.0 mmol) of CuI was added. The reaction mixture was stirred for 2 hr. at room temperature and then poured into approximately 100ml of a 10% HCl solution. The resulting precipitate was filtered, washed with water and dried. The solid was taken up in hot CHCl3 and filtered to remove insoluble salts. After evaporation of the solvent, the resulting orange solid was recrystallized from a chloroform-hexane mixture to produce a tan solid, m.p. 87-91°C.

Aufarbeitung

  1. additionwas added
  2. filtrationThe resulting precipitate was filtered
  3. washwashed with water
  4. customdried
  5. filtrationfiltered
  6. customto remove insoluble salts
  7. customAfter evaporation of the solvent
  8. customthe resulting orange solid was recrystallized from a chloroform-hexane mixture
  9. customto produce a tan solid, m.p. 87-91°C.

Quellen und Nachweise

ORD-Eintrag
ord-faa30264305d4ebdb1c8ba56d797c0bf
Quelldatensatz
uspto-grants-1989_08
Patentnummer
US04855324

Notizen zur Reaktion

Wird geladen…