Methyl iodide → HCID 19093551, compound

HRID 2166391Notes

Reaction equation

HRID 2166391 reaction equation
[C:1]([C:4]1[CH:9]=[C:8]([CH2:10][OH:11])[C:7]([O:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]#[N:18])=[CH:6][C:5]=1[O:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]#[N:25])(=[O:3])[CH3:2].[H-].[Na+].[CH3:28]I>CN(C)C=O>[C:1]([C:4]1[CH:9]=[C:8]([CH2:10][O:11][CH3:28])[C:7]([O:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]#[N:18])=[CH:6][C:5]=1[O:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]#[N:25])(=[O:3])[CH3:2]

Participants

5

Procedure

A mixture of 688 mg of 5,5'-[(4-acetyl-6-hydroxymethyl-1,3-phenylene)bis(oxy)]bis[pentanenitrile] in 15 ml of dimethylformamide was added to a suspension of 0.184 g of a 50 % oil dispersion of sodium hydride and 0.62 ml of methyl iodide in 45 ml of dimethylformamide at 0° C. The reaction was allowed to come to room temperature and stirred overnight. The reaction mixture was partitioned between ethyl acetate and dilute hydrochloric acid to which sodium chloride had been added. The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo. The resulting residue was purified by high pressure liquid chromatography over silica gel eluting with a 0-70% ethyl acetate in hexane gradient to provide 110 mg of the desired title product. NMR, MS.

Workup

  1. customto come to room temperature
  2. customThe reaction mixture was partitioned between ethyl acetate and dilute hydrochloric acid to which sodium chloride
  3. additionhad been added
  4. customThe organic layer was separated
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe resulting residue was purified by high pressure liquid chromatography over silica gel eluting with a 0-70% ethyl acetate in hexane gradient

Sources & evidence

ORD record
ord-e91d9d3a805649d5bcc4e203560aab0f
Source dataset
uspto-grants-1990_07
Patent number
US04945099

Reaction notes

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