Ethyl Acetate → HCID 19867638, compound

HRID 1720690Notes

Reaction equation

HRID 1720690 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:20][C:21](=O)[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:9]([C:15](=O)[CH:16]([CH3:18])[CH3:17])[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1.Cl.[NH2:30]O.[NH4+].[OH-].CCOC(C)=O>CC(O)=O.O.CCCCCC>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:20]=[C:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[N:30]=[C:15]([CH:16]([CH3:18])[CH3:17])[C:9]=2[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][CH:3]=1

Participants

8

Procedure

A mixture of β-(4-fluorophenyl)-α-(2-methyl-1-oxopropyl)-δ-oxobenzenepentanoic acid, ethyl ester (7.92 gm, 20.6 mmol) and hydroxylamine hydrochloride (4.32 gm, 62.2 mmol) in glacial HOAc (100 ml) was refluxed for 2.5 hours. The reaction was cooled to room temperature and poured into an ice cold solution of concentrated NH4OH (140 ml) in H2O (400 ml). The resulting mixture was extracted twice with Et2O and the combined ethereal layers were washed with brine, dried (Na2SO4), filtered and stripped to yield a gummy orange-red oil. Flash chromatography of the oil (Merck SiO2, 7% EtOAc in hexane) gave 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinecarboxylic acid, ethyl ester (4.88 gm, 65%) as a near colorless gum.

Workup

  1. temperaturewas refluxed for 2.5 hours
  2. extractionThe resulting mixture was extracted twice with Et2O
  3. washthe combined ethereal layers were washed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. customto yield a gummy orange-red oil

Sources & evidence

ORD record
ord-5edcc4becee047018c99bbb1349056f9
Source dataset
uspto-grants-1996_04
Patent number
US05506219

Reaction notes

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