Hydrochloric Acid → Methyl 3-chloro-4-hydroxyphenylacetate

HRID 351100Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 351100
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=[O:11])[CH:5]=[CH:6][C:7]=1[OH:8].Cl.[CH3:14]O>>[CH3:14][O:11][C:10](=[O:12])[CH2:9][C:4]1[CH:5]=[CH:6][C:7]([OH:8])=[C:2]([Cl:1])[CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a solution of 3-chloro-4-hydroxyphenyl acetic acid (20 mmol) in methanol (50 mL) was added concentrated HCl solution (5 mL), and stirred for 1 h at 50° C. After excess solvents were removed under vacuum, the residue was dissolved in EtOAc (50 mL) and washed with sat. NaHCO3 solution (2×30 mL), brine (30 mL) and dried over anhydrous Na2SO4. This afforded methyl 3-chloro-4-hydroxy acetate 3 as a colorless oil (4.0 g, 99%). 1H NMR (CDCl3) 6.9–7.0 (d, 1H), 6.8–6.9 (d, 1H), 5.4 (s, 1H), 3.6 (s, 3H), 3.4 (s, 2H).

Aufarbeitung

  1. customAfter excess solvents were removed under vacuum
  2. dissolutionthe residue was dissolved in EtOAc (50 mL)
  3. washwashed with sat. NaHCO3 solution (2×30 mL), brine (30 mL)
  4. dry with materialdried over anhydrous Na2SO4

Quellen und Nachweise

ORD-Eintrag
ord-87273c5935794d4589d4b181c70ffa5d
Quelldatensatz
uspto-grants-2007_02
Patentnummer
US07183307B2

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