Water → HCID 178482487, compound

HRID 544097Notes

Reaction equation

HRID 544097 reaction equation
[CH:1]([NH:3][C:4]1[CH2:8][CH2:7][N:6]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:10]=2)[N:5]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>C(OCC)C>[CH3:1][NH:3][C:4]1[CH2:8][CH2:7][N:6]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:16])[F:17])[CH:10]=2)[N:5]=1

Participants

5

Reactant 3

HCID 962WaterHCID 13306691HCID 13306691, compoundHCID 21226445Aluminium lithium hydride

Product 1

HCID 178482487HCID 178482487, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

3-Formamido-1-(3-trifluoromethylphenyl)-2-pyrazoline (2.4 g) was stirred with dry diethyl ether (60 ml) to produce a slurry which was gradually added to a stirred ice-cold suspension of lithium aluminum hydride (1.0 g) in dry diethyl ether (75 ml) under a nitrogen atmosphere. The addition took place over a period of about 20 minutes and was accompanied by a vigorous reaction. The final reaction mixture was stirred for a further 15 minutes and was then carefully and slowly decomposed by the addition of water (30 ml). The ethereal layer was then decanted off the aqueous sludge which was washed twice with diethyl ether. The combined ethereal solutions were dried over potassium carbonate, filtered and evaporated. The resulting 3-methylamino-1-(3-trifluoromethylphenyl)-2-pyrazoline was obtained as a colourless crystalline solid on trituration with benzene and recrystallization from light petroleum, yield 1.8 g, m.p. 93.1°. The hydrochloride was recrystallized by precipitation from methanol with ether and light petroleum m.p. 206°-207°.

Workup

  1. customto produce a slurry which
  2. additionThe addition
  3. customof about 20 minutes
  4. customwas accompanied by a vigorous reaction
  5. customThe final reaction mixture
  6. customThe ethereal layer was then decanted off the aqueous sludge which
  7. washwas washed twice with diethyl ether
  8. dry with materialThe combined ethereal solutions were dried over potassium carbonate
  9. filtrationfiltered
  10. customevaporated

Sources & evidence

ORD record
ord-647b35791d98456bb3bfdd9850e18a9f
Source dataset
uspto-grants-1984_05
Patent number
US04448783

Reaction notes

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