Ethanol → HCID 178490399, compound

HRID 273097

Reaction equation

HRID 273097 reaction equation
Cl.[NH2:2][OH:3].[OH-:4].[Na+].CO[C:8]1[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=1)[C:11]#[N:12].[CH2:16](O)C>>[OH:3][NH:2][C:11](=[NH:12])[C:10]1[CH:13]=[CH:14][CH:15]=[C:8]([O:4][CH3:16])[CH:9]=1

Participants

5

Conditions

Temperature
80 °C

Procedure

Using the general procedure of Shine et al., J. Heterocyclic Chem. (1989) 26:125-128, hydroxylamine hydrochloride (22 ml, 5 M, 110 mmol) and sodium hydroxide (11 ml, 10 M, 110 mmol) were added to a solution of 3-methoxybenzonitrile (11.5 ml. 94 mmol) in ethanol (130 ml). The reaction mixture was then heated at reflux (80° C.) for 12 h. After the mixture was cooled, most of the solvent was removed in vacuo. The crude product was partitioned between ethyl acetate and water, washed with saturated brine, dried over anhydrous sodium sulfate and the solvent was removed in vacuo. Flash chromatography on silica gel using 35-50% ethyl acetate in hexane yielded the title compound (8.05 g, 52%). Examples 7-9 were prepared in an analogous method to the procedure given in Example 6.

Workup

  1. temperatureThe reaction mixture was then heated
  2. temperatureAfter the mixture was cooled, most of the solvent
  3. customwas removed in vacuo
  4. customThe crude product was partitioned between ethyl acetate and water
  5. washwashed with saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-71e44e892b0b439d85e32a13d7a04c7a
Source dataset
uspto-grants-2008_11
Patent number
US07456200B2

Linked notes

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