1-Bromooctadecane → HCID 21185159, compound

HRID 1385478Notes

Reaction equation

HRID 1385478 reaction equation
[Na].[OH:2][C:3]1[CH:17]=[CH:16][C:6]([C:7]([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)=[O:8])=[CH:5][CH:4]=1.Br[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>C(O)C.[I-].[Na+]>[CH2:19]([O:2][C:3]1[CH:17]=[CH:16][C:6]([C:7]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH3:19])=[CH:11][CH:10]=2)=[O:8])=[CH:5][CH:4]=1)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]

Participants

6

Procedure

Sodium metal (0.46 g, 20 mmol) was dissolved in ethanol (50 mL) and 4,4′-dihydroxybenzophenone (1.0 g, 4.67 mmol) was added followed by 1-bromooctadecane (7.8 g, 23.4 mmol) and a catalytic amount of sodium iodide (approximately 30 mg) and the reaction mixture was refluxed for 48 hours. The resulting suspension was cooled and filtered. The solid was washed with dichloromethane followed by hexane and the white solid was dried to afford compound 22 (2.85 g, 84.8% yield). 1H NMR (300 MHz, pyridine-d5) δ 7.95 (d, J=8.7 Hz, 4 H, aryl), 7.09 (d, J=8.7 Hz, 4 H, aryl), 4.05 (t, J=6.6 Hz, 4 H, 2×OCH2), 1.80 (tt, J=6.6 and 7.5 Hz, 4 H), 1.48 (m, 4 H), 1.33 (brS, 60 H), 0.87 (t, J=6.6 Hz, 6 H, 2×CH3).

Workup

  1. temperatureThe resulting suspension was cooled
  2. filtrationfiltered
  3. washThe solid was washed with dichloromethane
  4. customthe white solid was dried

Sources & evidence

ORD record
ord-56cc367d62134f5fa906339c66042a13
Source dataset
uspto-grants-2001_07
Patent number
US06262251B1

Reaction notes

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