Pyridine → 1-Bromo-3,7,9-trimethyldeca-2,6-diene

HRID 596639

Reaktionsgleichung

Reaktionsgleichung von HRID 596639
[CH3:1][C:2](O)([CH2:5][CH2:6][CH:7]=[C:8]([CH3:13])[CH2:9][CH:10]([CH3:12])[CH3:11])[CH:3]=[CH2:4].N1C=CC=CC=1.P(Br)(Br)[Br:22]>CCCCCC>[Br:22][CH2:4][CH:3]=[C:2]([CH3:1])[CH2:5][CH2:6][CH:7]=[C:8]([CH3:13])[CH2:9][CH:10]([CH3:12])[CH3:11]

Komponenten

5

Versuchsvorschrift

19.8 g. of 3,7,9-trimethyl-1,6-decadien-3-ol, 100 ml. of hexane and 1 ml. of pyridine and cooled to -15° C. and treated dropwise over a period of 1.5 hours with a solution of 4 ml. of phosphorus tribromide in 50 ml. of hexane while maintaining the temperature between -15° and -10° C. The mixture is stirred for a further 90 minutes while slowly warming to room temperature. For the working-up, the mixture is poured on to 50 ml. of ice-water, the organic phase is separated and washed once with 20 ml. of 10% soda solution, once with 50 ml. of semi-saturated aqueous sodium chloride solution and once with 50 ml. saturated sodium chloride solution, dried over sodium sulphate and evaporated under reduced pressure. There is obtained 1-bromo-3,7,9-trimethyl-2,6-decadiene.

Aufarbeitung

  1. additiontreated dropwise over a period of 1.5 hours with a solution of 4 ml
  2. additionthe mixture is poured on to 50 ml
  3. customof ice-water, the organic phase is separated
  4. washwashed once with 20 ml
  5. dry with materialsaturated sodium chloride solution, dried over sodium sulphate
  6. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d4632101ccdb464f9dd9c1678292ae2e
Quelldatensatz
uspto-grants-1977_03
Patentnummer
US04011335

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