4-Chloro-3-methylphenol → 4-Chloro-1-(4-chloro-3-methylphenoxy)-2-butanol

HRID 1639054

Reaktionsgleichung

Reaktionsgleichung von HRID 1639054
[CH3:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[Cl:8].C(O)(C)(C)C.Cl[CH2:16][CH:17]([OH:21])[CH2:18][CH2:19][Cl:20].[OH-].[Na+]>O>[Cl:20][CH2:19][CH2:18][CH:17]([OH:21])[CH2:16][O:9][C:4]1[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([CH3:1])[CH:3]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

To a mixture of 286 g (2 mole) of 3-methyl-4-chlorophenol, 700 ml of tertiary butanol, 700 ml of water and 3.0 mole of 1,4-dichloro-2-butanol, sodium hydroxide (2.9 moles, 230 g in 700 ml of water) was added with stirring at 40° C. to maintain a pH of 9.5-10.0 as the reaction progressed. The addition was 10 hr; the reaction was stirred at 40° C. for 48 hr. The resulting reaction mixture was extracted with chloroform sodium hydroxide at 25° C. The chloroform extract was washed with sodium sulfate. The dried chloroform solution was concentrated and the residue was distilled under reduced pressure to give 110.9 g of the product which distilled at 135°-143° C./0.007 mm and melted at 87°-89° C. after recrystallization with isopropanol and petroleum ether (30°-60° C.).

Aufarbeitung

  1. additionwas added
  2. temperatureto maintain a pH of 9.5-10.0 as the reaction
  3. additionThe addition
  4. stirringthe reaction was stirred at 40° C. for 48 hr
  5. customThe resulting reaction mixture
  6. extractionwas extracted with chloroform sodium hydroxide at 25° C
  7. extractionThe chloroform extract
  8. washwas washed with sodium sulfate
  9. concentrationThe dried chloroform solution was concentrated
  10. distillationthe residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e6a02f8f2dde4a979e14dfca706495f2
Quelldatensatz
uspto-grants-1989_11
Patentnummer
US04882330

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