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Sulfuric Acid → Methyl 4-hydroxy-3-methylbenzoate

HRID 220819
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 220819
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7](N)=[C:6]([CH3:11])[CH:5]=1.S(=O)(=O)(O)[OH:14].N([O-])=O.[Na+].NC(N)=O>O.[N+]([O-])([O-])=O.[Cu+2].[N+]([O-])([O-])=O.[Cu]=O>[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([OH:14])=[C:6]([CH3:11])[CH:5]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 1118Sulfuric AcidHCID 1176UreaHCID 2736799Methyl 4-amino-3-methylbenzoateHCID 23668193Sodium Nitrite

Produkt 1

HCID 11240684Methyl 4-hydroxy-3-methylbenzoateAusbeute 42 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 14829
Copper oxide
Katalysator
HCID 18616Cupric nitrateKatalysator
HCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

4-Amino-3-methyl-benzoic acid methyl ester (5.25 g, 32.0 mmol) was treated with a 35% solution of sulphuric acid (50 ml) and the mixture was stirred and heated until dissolution then cooled to 0° C. Sodium nitrite (2.82 g, 41.6 mmol) in water (50 ml) was added dropwise and the mixture was stirred for 5 min at 0° C. Urea was added to destroy the excess nitrite. Copper nitrate (121 g, 320 mmol) in water (11) was added then copper oxide (4.25 g, 32.0 mmol). The mixture was warmed up to room temperature over 30 min and extracted with EtOAc (×3). The organics were combined, washed with brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 30% EtOAc:70% hexane) to yield the title compound (2.2 g, 42%).

Aufarbeitung

  1. temperatureheated until dissolution
  2. stirringthe mixture was stirred for 5 min at 0° C
  3. customto destroy the excess nitrite
  4. temperatureThe mixture was warmed up to room temperature over 30 min
  5. extractionextracted with EtOAc (×3)
  6. washwashed with brine
  7. customdried
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by flash chromatography on silica gel (eluant; 30% EtOAc:70% hexane)

Quellen und Nachweise

ORD-Eintrag
ord-c0232a661d8649d69561cda858228fa9
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08202858B2

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