Water → HCID 14820128, compound

HRID 487089Notes

Reaction equation

HRID 487089 reaction equation
[C:1]([C:4]1[C:16]([OH:17])=[CH:15][C:7]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]Br)=[C:6]([CH2:18][CH3:19])[CH:5]=1)(=[O:3])[CH3:2].N1C=[CH:23][N:22]=[N:21]1.C(=O)([O-])[O-].[K+].[K+].O.[CH3:32][N:33](C)C=O>>[CH2:18]([C:6]1[C:7]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:22]2[CH:23]=[N:33][CH:32]=[N:21]2)=[CH:15][C:16]([OH:17])=[C:4]([C:1](=[O:3])[CH3:2])[CH:5]=1)[CH3:19]

Participants

6

Conditions

Temperature
85 °C

Procedure

A mixture of 0.3 g of 5-(4-acetyl-2-ethyl-5-hydroxyphenoxy)pentyl bromide, 0.06 % of triazole, and 0.13 g of potassium carbonate in dimethylformamide was heated at 80-90° C. for approximately 18 hours. The mixture was poured into acidic water and extracted with ethyl acetate and methylene chloride. The extracts were combined, washed with dilute sodium hydroxide solution, dried over sodium sulfate, and concentrated in vacuo. The residue was twice crystallized from ethyl acetate/hexane to provide the title product having a melting point of 87° C.

Workup

  1. extractionextracted with ethyl acetate and methylene chloride
  2. washwashed with dilute sodium hydroxide solution
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was twice crystallized from ethyl acetate/hexane

Sources & evidence

ORD record
ord-3b90ea5f47344ea3a54d5adcd42e1a47
Source dataset
uspto-grants-1994_03
Patent number
US05294613

Reaction notes

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