Ammonium formate → HCID 72556533, compound

HRID 2238258Notes

Reaction equation

HRID 2238258 reaction equation
[O:1]=[C:2]1[NH:6][C:5](=[O:7])[C:4](=[CH:8][C:9]2[CH:33]=[CH:32][C:12]([O:13][C:14]3[CH:19]=[CH:18][C:17]([C:20](=[CH:24][C:25]4[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=4)[C:21]([OH:23])=[O:22])=[CH:16][CH:15]=3)=[CH:11][CH:10]=2)[S:3]1.C([O-])=O.[NH4+]>C(O)(=O)C.[Pd]>[O:1]=[C:2]1[NH:6][C:5](=[O:7])[CH:4]([CH2:8][C:9]2[CH:10]=[CH:11][C:12]([O:13][C:14]3[CH:15]=[CH:16][C:17]([C:20](=[CH:24][C:25]4[CH:26]=[CH:27][C:28]([CH3:31])=[CH:29][CH:30]=4)[C:21]([OH:23])=[O:22])=[CH:18][CH:19]=3)=[CH:32][CH:33]=2)[S:3]1

Participants

5

Reactant 2

HCID 2723923Ammonium formateHCID 725565302-{4-[4-(2,4-Dioxothiazolidin-5-ylidenemethyl)-phenoxy]-phenyl}-3-p-tolylacrylic acid

Product 1

HCID 72556533HCID 72556533, compoundYield 60.2%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 176Acetic AcidSolvent

Procedure

To a solution of 40 (1.0 g, 2.2 mmol) and ammonium formate (8.32 g, 132 mmol) in 25 mL glacial acetic acid was added 5% Pd/C (1.0 g). The mixture was refluxed for 7.5 h, cooled to room temperature and filtered over Celite. The mixture was concentrated in vacuum then added to 200 mL water. The product was filtered and washed with hexanes. The solid was recrystallized out of toluene, cooled to room temperature and sonicated until the solid was observed. The mixture was then stirred at room temperature for 16 h. The precipitate was collected and washed with hexanes to yield a white solid (0.609 g, 59.1%). 1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1H), 12.05 (br s, 1H), 7.72 (s, 1H), 7.30 (d, J=8.8 Hz, 2H), 7.16 (d, J=8.4 Hz, 2H), 7.05 (d, J=8.4 Hz, 2H), 7.01 (d, J=8.4 Hz, 2H), 6.99 (d, J=9.2 Hz, 2H), 6.98 (d, J=8.0 Hz, 2H), 4.92 (dd, J=4.4 and 9.6 Hz, 1H), 3.38 (dd, J=4.4 and 14.0 Hz, 1H), 3.21 (dd, J=9.2 and 14.0 Hz, 1H), 2.24 (s, H).

Workup

  1. temperatureThe mixture was refluxed for 7.5 h
  2. filtrationfiltered over Celite
  3. concentrationThe mixture was concentrated in vacuum
  4. additionthen added to 200 mL water
  5. filtrationThe product was filtered
  6. washwashed with hexanes
  7. customThe solid was recrystallized out of toluene
  8. temperaturecooled to room temperature
  9. customsonicated until the solid
  10. customThe precipitate was collected
  11. washwashed with hexanes

Sources & evidence

ORD record
ord-9b3c15fe77694bdd817c5933aee7b15e
Source dataset
uspto-grants-2010_05
Patent number
US07718682B2

Reaction notes

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