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Boron Trichloride → Benzoic acid, 2-hydroxy-4-methoxy-6-methyl-, ethyl ester

HRID 2100623
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2100623
C[O:2][C:3]1[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[C:10]([CH3:16])[C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6].B(Cl)(Cl)Cl>C(Cl)Cl>[OH:2][C:3]1[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[C:10]([CH3:16])[C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 25135Boron TrichlorideHCID 4343031ethyl 2,4-dimethoxy-6-methylbenzoate

Produkt 1

HCID 80201Benzoic acid, 2-hydroxy-4-methoxy-6-methyl-, ethyl esterAusbeute 70,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of ethyl 2,4-dimethoxy-6-methylbenzoate (5.73 g, 25.6 mmol) in 200 mL of methylene chloride at −78° C. was added boron trichloride (28.1 mL of a 1.0 M solution in methylene chloride, 28.1 mmol) via an addition funnel over 15 min. The solution was allowed to stir at −78° C. for 2 h. The cooling bath was removed, the reaction was allowed to warm for 15 min. and then was carefully quenched with 1N HCl. Most of the methylene chloride was removed by rotary evaporator and the reaction was diluted with ethyl acetate. The organics were washed with 1N HCl and brine, dried (MgSO4) and concentrated. The residue was purified by flash chromatography (elution with 8:1 hexane/ethyl acetate) to afford 3.8 g (70%) of the title compound as a tan solid. 1H NMR (CDCl3): δ 11.85 (s, 1H), 6.31 (d, 1H, J=2.2 Hz), 6.25 (d, 1H, J=2.6 Hz), 4.37 (q, 2H, J=7.2 Hz), 3.77 (s, 3H), 2.49 (s, 3H), 1.39 (t, 3H, J=7.4 Hz).

Aufarbeitung

  1. customThe cooling bath was removed
  2. temperatureto warm for 15 min.
  3. customwas carefully quenched with 1N HCl
  4. customMost of the methylene chloride was removed by rotary evaporator
  5. additionthe reaction was diluted with ethyl acetate
  6. washThe organics were washed with 1N HCl and brine
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customThe residue was purified by flash chromatography (elution with 8:1 hexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-ae38d5cfff1642f6a9efc7db416d524f
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07572805B2

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