Ethylene Glycol → HCID 21925647, compound

HRID 2118019Notes

Reaction equation

HRID 2118019 reaction equation
[H-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[C:6](F)[CH:5]=1.[CH2:14]([OH:17])[CH2:15][OH:16]>CN1CCCC1=O>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[C:6]([CH:5]=1)[O:16][CH2:15][CH2:14][OH:17]

Participants

5

Conditions

Temperature
80 °C

Procedure

Sodium hydride (125 mg, 60% dispersion in mineral oil, 3.13 mmol) was added to a mixture of 4-chloro-2-fluoronitrobenzene (500 mg, 2.85 mmol) and ethylene glycol (0.18 ml, 3.13 mmol) in 1-methyl-2-pyrrolidinone (5 ml) and the reaction stirred at 80° C. for 18 hours. TLC analysis showed starting material remaining, so additional sodium hydride (114 mg, 60% dispersion in mineral oil, 2.85 mmol) and ethylene glycol (0.82 ml, 14.25 mmol) were added and the reaction stirred at 110° C. for a further 18 hours. The cooled mixture was partitioned between water and dichloromethane, and the layers separated. The organic phase was dried over magnesium sulphate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate:pentane (50:50) as eluant to afford the title compound as a solid, 290 mg.

Workup

  1. stirringthe reaction stirred at 110° C. for a further 18 hours
  2. customThe cooled mixture was partitioned between water and dichloromethane
  3. customthe layers separated
  4. dry with materialThe organic phase was dried over magnesium sulphate
  5. customevaporated under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-81eec630f96d4fe6af21cd4b30e6f066
Source dataset
uspto-grants-2008_10
Patent number
US07442795B2

Reaction notes

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