Phosphoric Acid → 2,4-Dimethylresorcinol

HRID 743955

Reaction equation

HRID 743955 reaction equation
[OH:1][C:2]1[C:9]([CH3:10])=[C:8]([OH:11])[CH:7]=[CH:6][C:3]=1[CH:4]=O.P(=O)(O)(O)O>[Pd].C(O)(C)C>[CH3:10][C:9]1[C:2]([OH:1])=[C:3]([CH3:4])[CH:6]=[CH:7][C:8]=1[OH:11]

Participants

5

Procedure

A solution of 2,4-dihydroxy-3-methylbenzaldehyde (30.0 g, 197 mmol) with isopropanol (3 L) was ice-cooled in a 5 L 3-neck flask fitted with a magnetic stirrer. Phosphoric acid (4 mL) and 10% palladium on carbon were added and the solution was sparged with nitrogen, then hydrogen. When uptake was judged to be complete (c. 1.5 hour) the solution was again sparged with nitrogen and then filtered through Celite®. The solvent was stripped off, the residue taken up in ethyl acetate, and the resulting solution washed with water (4×100 mL). The water washes were back-extracted with ethyl acetate and the combined organic layers dried over sodium sulfate and stripped down. Sublimation (95°, 0.05 torr) afforded a colorless solid (19.6 g, 72%). M.p. 107°-8° C. (Lit. 108°-109° C. [W. Baker et al., J. Chem. Soc., 2834-5 (1949).]). NMR (DMSO-d6): δ1.969 (s, 3H), 2.037 (s, 3H), 6.220 (d, J=8.1 hz, 1H), 6.637 (d, J=8.1 hz, 1H), 7.929 (s, 1H), and 8.785 (s, 1H).

Workup

  1. temperaturecooled in a 5 L 3-neck flask
  2. customfitted with a magnetic stirrer
  3. customthe solution was sparged with nitrogen
  4. custom(c. 1.5 hour)
  5. customwas again sparged with nitrogen
  6. filtrationfiltered through Celite®
  7. washthe resulting solution washed with water (4×100 mL)
  8. extractionThe water washes were back-extracted with ethyl acetate
  9. dry with materialthe combined organic layers dried over sodium sulfate

Sources & evidence

ORD record
ord-da2406d6e6bf464d8dcf022e85b2f7d2
Source dataset
uspto-grants-1996_09
Patent number
US05558991

Linked notes

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