Water → HCID 70170307, compound

HRID 635493Notes

Reaction equation

HRID 635493 reaction equation
[H-].[Na+].[C:3]([O:6][CH2:7][C:8]([NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])([CH2:18][CH3:19])[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)(=[O:5])[CH3:4].[C:28]1([CH2:34][CH2:35][CH2:36][CH2:37]I)[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.O>CN(C)C=O>[C:3]([O:6][CH2:7][C:8]([NH:20][C:21]([O:23][C:24]([CH3:26])([CH3:25])[CH3:27])=[O:22])([CH2:18][CH3:19])[CH2:9][CH2:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][CH2:37][CH2:36][CH2:35][CH2:34][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[CH:15][CH:16]=1)(=[O:5])[CH3:4]

Participants

6

Procedure

To a suspension of sodium hydride (0.65 g) in dimethylformamide (16 ml) was added a solution of 2-tert-butoxycarbonylamino-2-ethyl-4-(4-hydroxyphenyl)butyl acetate (6.0 g) in dimethylformamide (50 ml) at 0° C. and the mixture was stirred at room temperature for an hour. 4-Phenyl-butyl iodide (90 g) was added to the solution at 0° C. and the mixture was allowed to stand at room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and a saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=1:1) to give the subject compound (3.6 g).

Workup

  1. extractionextracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with water
  3. dry with materiala saturated brine and dried over anhydrous sodium sulfate
  4. distillationThe solvent was distilled away under reduced pressure
  5. customthe residue obtained
  6. customwas purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=1:1)

Sources & evidence

ORD record
ord-05729fbce3734184aad405bbee01d3a1
Source dataset
uspto-grants-2001_02
Patent number
US06187821B1

Reaction notes

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