Ethyl Bromide → HCID 22618612, compound

HRID 2253793Notes

Reaction equation

HRID 2253793 reaction equation
[CH2:1]([Mg]Br)[CH3:2].[Mg].C(Br)C.[NH2:9][C:10]1[N:14]([C:15]2[C:20]([Cl:21])=[CH:19][C:18]([C:22]([F:25])([F:24])[F:23])=[CH:17][C:16]=2[Cl:26])[N:13]=[C:12]([C:27]([F:30])([F:29])[F:28])[C:11]=1[S:31]C#N>C(OCC)C.O>[NH2:9][C:10]1[N:14]([C:15]2[C:20]([Cl:21])=[CH:19][C:18]([C:22]([F:23])([F:24])[F:25])=[CH:17][C:16]=2[Cl:26])[N:13]=[C:12]([C:27]([F:28])([F:30])[F:29])[C:11]=1[S:31][CH2:1][CH3:2]

Participants

7

Procedure

A solution of ethyl magnesium bromide, prepared from magnesium (0.57 g) and ethyl bromide (2.6 g) in dry diethyl ether (25 ml), was added dropwise to a stirred solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-thiocyanato-3-trifluoromethylpyrazole (5.0 g) in dry ether (50 ml) at -20° C. After stirring for a further 2 hours at room temperature, water (130 ml) was carefully added, and stirring maintained for 0.25 hour. The ether layer was separated, dried over anhydrous magnesium sulphate, and evaporated in vacuo to give a yellow gum. Purification by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm-2) eluting with dichloromethane-petroleum ether (1:1) gave a product, which recrystallized from hexane to furnish 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethylthio-3-trifluoromethylpyrazole, in the form of white needles, m.p. 116°-116.5° C.

Workup

  1. stirringstirring
  2. temperaturemaintained for 0.25 hour
  3. customThe ether layer was separated
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customevaporated in vacuo
  6. customto give a yellow gum
  7. customPurification by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm-2)
  8. washeluting with dichloromethane-petroleum ether (1:1)
  9. customgave a product, which
  10. customrecrystallized from hexane

Sources & evidence

ORD record
ord-61082c217c7c4ddea7cd137d679cc14e
Source dataset
uspto-grants-1993_08
Patent number
US05232940

Reaction notes

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