p-Toluenesulfonic acid → HCID 23507821, compound

HRID 2289272Notes

Reaction equation

HRID 2289272 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=[O:16])[CH2:11][CH2:12][C:13]([OH:15])=[O:14])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:17](O)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28].C1(C)C=CC(S(O)(=O)=O)=CC=1>O1CCCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10](=[O:16])[CH2:11][CH2:12][C:13]([O:15][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH3:17])=[O:14])=[CH:8][CH:9]=1)([O-:3])=[O:2]

Participants

5

Procedure

A solution of 4-(4-nitrophenyl)-4-oxobutyric acid (0.50 g, 2.2 mmol), 1-dodecanol (5.0 ml, 22 mmol), and p-toluenesulfonic acid (50 mg) in tetrahydrofuran (2.5 ml) was stirred 60 hours at room temperature then heated under reflux for 1.5 hours. Concentration of the reaction mixture in vacuo and purification by chromatography or silica gel (200 g) eluting with methylene chloride:hexane (1.1 to 2:1) followed by filtration of the solid product from a small volume of hexane gave, after drying under high vacuum, dodecyl 4-(4-nitrophenyl)-4-oxobutyrate (0.43 g) as a white solid. 1H NMR (DMSO-66, 300 MHz) δ:

Workup

  1. temperaturethen heated
  2. temperatureunder reflux for 1.5 hours
  3. customConcentration of the reaction mixture in vacuo and purification by chromatography or silica gel (200 g)
  4. washeluting with methylene chloride
  5. filtrationhexane (1.1 to 2:1) followed by filtration of the solid product from a small volume of hexane
  6. customgave
  7. dry with materialafter drying under high vacuum, dodecyl 4-(4-nitrophenyl)-4-oxobutyrate (0.43 g) as a white solid

Sources & evidence

ORD record
ord-eb8442a922844d1283584f4141c33acb
Source dataset
uspto-grants-2000_07
Patent number
US06090941

Reaction notes

Loading…