Ammonium Hydroxide → HCID 13127496, compound

HRID 2413092Notes

Reaction equation

HRID 2413092 reaction equation
[Cl:1][C:2]1[CH:8]=[C:7]([CH2:9][CH3:10])[CH:6]=[CH:5][C:3]=1[NH2:4].[N:11]([O-])=O.[Na+].[OH-].[NH4+]>C(O)(=O)C.S(=O)(=O)(O)O.Cl>[Cl:1][C:2]1[CH:8]=[C:7]([CH2:9][CH3:10])[CH:6]=[CH:5][C:3]=1[NH:4][NH2:11]

Participants

7

Procedure

2-Chloro-4-ethylaniline [14.5 g; described by K. Altau, J. Chem. Eng. Data, 8, 122 (1963)] was dissolved, with stirring, in glacial acetic acid (113 ml). A solution of sodium nitrite (7.0 g) in concentrated sulphuric acid (55 ml) was then added at 55°-60° C. The solution thus obtained was cooled to 0°-5° C. and a solution of stannous chloride (70 g) in concentrated hydrochloric acid (80 ml) was added with vigorous stirring. A cream-coloured solid precipitated. The mixture was filtered and the solid obtained was added to a mixture of aqueous ammonium hydroxide solution and ice. The mixture thus obtained was extracted with diethyl ether (4×300 ml) and the combined ethereal extracts were dried over sodium sulphate, filtered and evaporated to dryness, to give 2-chloro-4-ethylphenylhydrazine (9.6 g), m.p. 55°-57° C., in the form of a cream-coloured solid.

Workup

  1. customThe solution thus obtained
  2. temperaturewas cooled to 0°-5° C.
  3. customA cream-coloured solid precipitated
  4. filtrationThe mixture was filtered
  5. customthe solid obtained
  6. customThe mixture thus obtained
  7. extractionwas extracted with diethyl ether (4×300 ml)
  8. dry with materialthe combined ethereal extracts were dried over sodium sulphate
  9. filtrationfiltered
  10. customevaporated to dryness

Sources & evidence

ORD record
ord-ba79d5ac84dc44448549e960bfef43ea
Source dataset
uspto-grants-1985_01
Patent number
US04496390

Reaction notes

Loading…