Acetic Acid → 1-Phenyl-3-acetoxybutane

HRID 274171

Reaktionsgleichung

Reaktionsgleichung von HRID 274171
[C:1]1([CH2:7][CH2:8][CH:9]([OH:11])[CH3:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(C)C=CC=CC=1.[C:19](O)(=[O:21])[CH3:20].Cl>CN(C)C1C=CN=CC=1.N1C=CC=CC=1>[C:19]([O:11][CH:9]([CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH3:10])(=[O:21])[CH3:20]

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 1140TolueneHCID 613024-Phenyl-2-butanol

Produkt 1

HCID 615171-Phenyl-3-acetoxybutaneAusbeute 98,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 1049PyridineLösungsmittel

Versuchsvorschrift

Into a four-necked flask provided with a thermometer and a stirrer, 150 g (1 mol) of 4-phenyl-2-butanol (XXX-35), 500 ml of toluene and 200 ml of pyridine were charged. 122.4 g (1.2 mol) of anhydrous acetic acid and 1 g of 4-dimethylaminopyridine were further added thereto to react them for 4 hours, while temperature being maintained at 40°-50° C. After completion of the reaction, the reaction mixture was poured into 500 ml of 4N hydrochloric acid solution, extracted and fractionated, and then an organic layer was washed with 1N hydrochloric acid, water, 5% sodium bicarbonate solution and water in the order. The thus-obtained Organic layer was concentrated under a reduced pressure to obtain 189 g of 2-acetoxy-4-phenylbutane (XXIX-35) with yield of 98.5%.

Aufarbeitung

  1. additionwere charged
  2. customto react them for 4 hours
  3. temperaturewhile temperature being maintained at 40°-50° C
  4. customAfter completion of the reaction
  5. extractionextracted
  6. washan organic layer was washed with 1N hydrochloric acid, water, 5% sodium bicarbonate solution and water in the order
  7. concentrationThe thus-obtained Organic layer was concentrated under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-4a027c600c1b409fa64f0e264bc8a4d8
Quelldatensatz
uspto-grants-1995_02
Patentnummer
US05389293

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