Phosphoric Acid → 1,3-Benzenediol, 4-methyl-

HRID 55713

Reaktionsgleichung

Reaktionsgleichung von HRID 55713
[OH:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=O.P(=O)(O)(O)O>CC(O)C.[Pd]>[CH3:4][C:3]1[CH:6]=[CH:7][C:8]([OH:10])=[CH:9][C:2]=1[OH:1]

Komponenten

5

Versuchsvorschrift

2,4-Dihydroxybenzaldehyde (33.97 gm, 0.246 mol) (recrystallized from toluene) was dissolved in spectroscopic grade 2-propanol (3 L) in a round bottom flask fitted with a gas inlet and a bubbler outlet. 10% Palladium on carbon (1.35 gm) was added followed by phosphoric acid (3 mL) and the mixture was sparged with nitrogen. The nitrogen flow was switched to hydrogen and the mixture was rapidly stirred with ice cooling. After 3 hours hydrogen uptake was complete and the catalyst was removed by filtration. The filtrate was stripped down to 200 mL and 200 mL of ethyl acetate was added. The solution was washed with 4×200 mL of water and the combined water extracts back-extracted with ethyl acetate. These organic extracts were water washed and the combined organic layers dried over sodium sulfate and striped down to afford the product as a colorless crystalline solid (29.95 gm, 98%). M.p.: 106° C. (Lit. 106°-107° C. [J. C. Bell, W. Bridge, and A. Robertson, J. Chem. Soc., 1542-45 (1937)]).

Aufarbeitung

  1. customfitted with a gas inlet and a bubbler outlet
  2. customthe mixture was sparged with nitrogen
  3. customthe catalyst was removed by filtration
  4. additionwas added
  5. washThe solution was washed with 4×200 mL of water
  6. extractionthe combined water extracts back-extracted with ethyl acetate
  7. washwashed
  8. dry with materialthe combined organic layers dried over sodium sulfate

Quellen und Nachweise

ORD-Eintrag
ord-828bdc66e947456a81985c2b2a4c16c9
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05625081

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