Phenol → 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide

HRID 378597

Reaction equation

HRID 378597 reaction equation
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([O:6][CH2:7][CH2:8][C:9]([OH:11])=O)=[CH:4][CH:3]=1.ClC1C=CC(O)=CC=1.C1(O)C=CC=CC=1.O(CCC(O)=O)C1C=CC=CC=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[NH2:53][CH2:54][CH2:55][CH2:56][N:57]1[CH:61]=[CH:60][N:59]=[CH:58]1>C1COCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][CH2:8][C:9]([NH:53][CH2:54][CH2:55][CH2:56][N:57]2[CH:61]=[CH:60][N:59]=[CH:58]2)=[O:11])=[CH:12][CH:13]=1

Participants

8

Procedure

A solution of 3-(4-chlorophenoxy)propionic acid (5.0 g, prepared from 4-chlorophenol by the process described in J.A.C.S. 1923, 2708 for the conversion of phenol into 3-phenoxypropionic acid) in THF (90 ml) was treated with 1,1'-carbonyldiimidazole (4.05 g) at room temperature with stirring. The mixture was stirred at ambient temperature for two hours. 1-(3-Aminopropyl)imidazole (3.12 g) was added and the mixture was stirred at ambient temperature for 18 hours. The solvent was distilled off and the residue was dissolved in dichloromethane, washed with water, dried and then evaporated to give a solid which was recrystallised from ethyl acetate to give 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide, m.p. 114-115.5° C.

Workup

  1. stirringThe mixture was stirred at ambient temperature for two hours
  2. stirringthe mixture was stirred at ambient temperature for 18 hours
  3. distillationThe solvent was distilled off
  4. dissolutionthe residue was dissolved in dichloromethane
  5. washwashed with water
  6. customdried
  7. customevaporated
  8. customto give a solid which
  9. customwas recrystallised from ethyl acetate

Sources & evidence

ORD record
ord-133c6d49555047b9ace0b93851c7481d
Source dataset
uspto-grants-2000_02
Patent number
US06031109

Linked notes

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