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Methanol → (4-Nitro-1,2-phenylene)dimethanol

HRID 550970
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 550970
[N+:1]([C:4]1[CH:5]=[C:6]([C:13](O)=[O:14])[C:7](=[CH:11][CH:12]=1)[C:8](O)=[O:9])([O-:3])=[O:2].CO>O1CCCC1>[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][OH:9])=[C:6]([CH2:13][OH:14])[CH:5]=1)([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 887MethanolHCID 691211,2-Benzenedicarboxylic acid, 4-nitro-

Produkt 1

HCID 11019518(4-Nitro-1,2-phenylene)dimethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

4-Nitrophthalic acid (40 g, 189.5 mmol) in tetrahydrofuran (500 mL) was added dropwise over 1.5 h to a solution of borane-THF complex (1 M, 490 mL, 490 mmol), keeping the reaction temperature between 0° C. and 5° C. After the addition, the reaction was allowed to warm slowly to ambient temperature and stirred for 18 h. Methanol (100 mL) was added carefully and the precipitated solid dissolved. The mixture was concentrated in vacuo to about 500 mL, cooled to 0° C., and 10 N sodium hydroxide was added to adjust the pH to 10-11. This mixture was extracted with EtOAc (3×600 mL) and the combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=207 (M−OH+CH3CN).

Aufarbeitung

  1. customthe reaction temperature between 0° C. and 5° C
  2. additionAfter the addition
  3. dissolutionthe precipitated solid dissolved
  4. concentrationThe mixture was concentrated in vacuo to about 500 mL
  5. temperaturecooled to 0° C.
  6. addition10 N sodium hydroxide was added
  7. extractionThis mixture was extracted with EtOAc (3×600 mL)
  8. washthe combined organic layers were washed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3819a338e79f4b8c9b24d0db73db35a0
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07947677B2

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