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Hydrochloric Acid → Methyl (2-hydroxyphenyl)acetate

HRID 129705
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 129705
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10].Cl.[CH3:13]O>>[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([O:11][CH3:13])=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11970(2-Hydroxyphenyl)acetic acid

Produkt 1

HCID 89719Methyl (2-hydroxyphenyl)acetateAusbeute 92 %

Versuchsvorschrift

2-(Hydroxyphenyl)acetic acid (50 g) was added to a solution of hydrogen chloride in methanol [prepared from acetyl chloride (25 ml) and methanol (250 ml)]. The solution was stirred at room temperature for three hours and then allowed to stand overnight (fifteen hours). The resulting mixture was concentrated under reduced pressure, and the residue was taken up in ether (250 ml) and washed with an aqueous solution of sodium bicarbonate until effervescence ceased. The ethereal solution was dried and then concentrated under reduced pressure and the resulting solid was recrystallized from ether/petrol to afford methyl (2-hydroxyphenyl)acetate (50 g; 92% yield) as white, powdery crystals, top. 70°-72° C.; infrared max. (nujol mull): 3420, 1715 cm-1 ; 1H nmr (90 MHz): delta 3.70 (2H,s), 3.75 (3H,s), 6.80-6.95 (2H,m), 7.05-7.10 (1H,m), 7.15-7.25 (1H,m), 7.40 (1H, s) ppm.

Aufarbeitung

  1. waitto stand overnight
  2. custom(fifteen hours)
  3. concentrationThe resulting mixture was concentrated under reduced pressure
  4. washwashed with an aqueous solution of sodium bicarbonate until effervescence
  5. customThe ethereal solution was dried
  6. concentrationconcentrated under reduced pressure
  7. customthe resulting solid was recrystallized from ether/petrol

Quellen und Nachweise

ORD-Eintrag
ord-ddcf66038df241f09c6266db14ccbd6a
Quelldatensatz
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05470819

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