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Potassium Carbonate → HCID 59560832, compound

HRID 1176964
Notes
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Reaction equation

HRID 1176964 reaction equation
[C:1]([O-])([O-])=O.[K+].[K+].[CH2:7]([O:19][C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][C:27]=1[O:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])[CH:23]=O)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]>O1CCOCC1.O>[CH2:29]([O:28][C:27]1[CH:26]=[CH:25][C:22]([CH:23]=[CH2:1])=[CH:21][C:20]=1[O:19][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 11430Potassium CarbonateHCID 27249313,4-Bis(dodecyloxy)benzaldehyde

Product 1

HCID 59560832HCID 59560832, compoundYield 65.6%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 312751,4-DioxaneSolvent

Conditions

Temperature
95 °C

Procedure

A round bottom flask was charged with Ph3PMeBr (8.79 g, 24.6 mmol), K2CO3 (3.4 g, 24.6 mmol), and 3,4-bis-dodecyloxy-benzaldehyde (10.0 g, 21.1 mmol) in a mixture of 25 mL of 1,4-dioxane and 0.3 mL of H2O. The reaction mixture was refluxed at 95° C. for 24 h. The reaction mixture was allowed to cool down to room temperature and extracted with CH2Cl2. The organic layer was washed with H2O and dried over anhydrous MgSO4. The solvent was removed under reduced pressure to give an off-white solid. The crude product was purified by column chromatography (silica gel, hexanes:dichloromethane=2:1 (v/v)) to give a white solid (6.53 g, 65.6%). 1H NMR (300 MHz, CDCl3, δ): 6.96 (d, J=1.9 Hz, 1H), 6.90 (dd, J=8.0 Hz, 1.9 Hz, 1H), 6.80 (d, J=8.2 Hz, 1H), 6.62 (dd, J=17.3 Hz, 10.7 Hz, 1H), 5.57 (dd, J=17.6 Hz, 0.5 Hz, 1H), 5.11 (d, J=11.5 Hz, 1H), 3.98 (q, J=6.6 Hz, 4H), 1.74-1.85 (m, 4H), 1.19-1.50 (m, 36H), 0.87 (t, J=6.6 Hz, 6H). 13C{1H} NMR (75 MHz, CDCl3, δ): 149.01, 148.98, 136.44, 130.63, 119.46, 113.44, 111.50, 111.18, 69.24, 32.00, 29.78, 29.72, 29.51, 29.45, 29.38, 29.34, 26.12, 22.78, 14.22. HRMS-EI (m/z): [M]+ calcd for C32H56O2, 472.4280; found, 472.4267. Anal. Calcd C32H56O2: C, 81.29; H, 11.94. Found: C, 81.36; H, 11.99.

Workup

  1. temperatureto cool down to room temperature
  2. extractionextracted with CH2Cl2
  3. washThe organic layer was washed with H2O
  4. dry with materialdried over anhydrous MgSO4
  5. customThe solvent was removed under reduced pressure
  6. customto give an off-white solid
  7. customThe crude product was purified by column chromatography (silica gel, hexanes:dichloromethane=2:1 (v/v))

Sources & evidence

ORD record
ord-37d1f87ced7d4d0dbac4d0ab75eee2af
Source dataset
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07842830B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes