Ethyl Bromide → HCID 22618612, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 2
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
- stirringstirring
- temperaturemaintained for 0.25 hour
- customThe ether layer was separated
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated in vacuo
- customto give a yellow gum
- customPurification by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm−2)
- washeluting with dichloromethane-petroleum ether (1:1)
- customgave a product, which
- customrecrystallized from hexane
Sources & evidence
- ORD record
- ord-356844d7da734815a58fda0e60c630c3
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372774B1
Reaction notes
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