Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1) → 1-(4-Chlorophenyl)-1-(2-cyclopentylethyl)hydrazine

HRID 2198329Notes

Reaction equation

HRID 2198329 reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH2:10])=[CH:5][CH:4]=1.Br[CH2:12][CH2:13][CH:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.[OH-].[Na+].O>[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH2:12][CH2:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)[NH2:10])=[CH:5][CH:4]=1

Participants

6

Reactant 2

HCID 71600Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 12711948(2-Bromoethyl)cyclopentane

Product 1

HCID 669116271-(4-Chlorophenyl)-1-(2-cyclopentylethyl)hydrazineYield 55%

Reagents, catalysts & solvents 3

HCID 70681Tetrabutylammonium ChlorideCatalystHCID 962WaterSolventHCID 14798Sodium HydroxideSolvent

Conditions

Temperature
60 °C

Procedure

4-Chlorophenylhydrazine hydrochloride (1.65 g, 9 mmol) was added to a vigorously stirred mixture of tetra-n-butylammonium chloride (0.126 g, 0.45 mmol) in 50% aqueous sodium hydroxide (9 mL) followed by (2-bromo-ethyl)-cyclopentane (1.74 g, 9.9 mmol). The reaction was heated to 60° C. (oil bath temperature) for 8 h. The reaction was cooled, diluted with water (75 mL) and extracted with chloroform (3×30 mL). The combined organic layer was dried (Na2SO4), filtered and concentrated under reduced pressure to an orange oil (0.69 g). The oil was subjected to column chromatography (silica gel, eluent: 50% dichloromethane in hexane followed by 70% dichloromethane in hexane) to give a yellow oil (1.17 g, 55%).

Workup

  1. temperatureThe reaction was cooled
  2. extractionextracted with chloroform (3×30 mL)
  3. dry with materialThe combined organic layer was dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure to an orange oil (0.69 g)

Sources & evidence

ORD record
ord-2a368da8338645188f9c7514736a4175
Source dataset
uspto-grants-2012_12
Patent number
US08338447B2

Reaction notes

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