2-Chloroacrylonitrile → 1-tert-Butyl-1H-pyrazol-3-amine

HRID 1755294Notes

Reaction equation

HRID 1755294 reaction equation
[C:1]([NH:5][NH2:6])([CH3:4])([CH3:3])[CH3:2].Cl[C:8](=[CH2:11])[C:9]#[N:10].CC([O-])=O.[Na+]>C(O)C>[C:1]([N:5]1[CH:11]=[CH:8][C:9]([NH2:10])=[N:6]1)([CH3:4])([CH3:3])[CH3:2]

Participants

5

Conditions

Temperature
80 °C

Procedure

A mixture of tert-butylhydrazine (2.4 g, 27 mmol), 2-chloroacrylonitrile (2.9 g, 33 mmol), NaOAc (3.17 g, 38 mmol) and ethanol (30 mL) was heated to 80° C. with stirring for 12 h. The solvent was removed in vacuo and the resulting mixture was treated with saturated NaHCO3 solution (200 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were dried over NaSO4, concentrated in vacuo, purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=2:1 to 1:2) to give 1-tert-butyl-1H-pyrazol-3-amine (1.39 g, 37%) as a brown oil. LC-MS: [M+H]+, 140.2, tR=0.696 min.

Workup

  1. customThe solvent was removed in vacuo
  2. additionthe resulting mixture was treated with saturated NaHCO3 solution (200 mL)
  3. extractionextracted with ethyl acetate (200 mL×3)
  4. dry with materialThe organic layers were dried over NaSO4
  5. concentrationconcentrated in vacuo
  6. custompurified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=2:1 to 1:2)

Sources & evidence

ORD record
ord-5830c03ebfdc46859f6eed8d2db7a0ba
Source dataset
uspto-grants-2015_10
Patent number
US09169259B2

Reaction notes

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