4-Chlorobenzaldehyde → anti-p-Chlorobenzaldoxime

HRID 1911653Notes

Reaction equation

HRID 1911653 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.Cl.[NH2:11][OH:12].[OH-].[Na+]>C(O)C.O>[Cl:1][C:2]1[CH:9]=[CH:8][C:5](/[CH:6]=[N:11]\[OH:12])=[CH:4][CH:3]=1

Participants

6

Procedure

To a suspension of 4-chlorobenzaldehyde (25.0 g, 178 mmol) and hydroxylamine hydrochloride (13.7 g, 198 mmol) in ethanol (14.2 mL) and water (42.9 mL) was added ice (82.4 g). Then a solution of sodium hydroxide (18.1 g, 455 mmol) in water (21.4 mL) was added dropwise within a 10 min period (temperature rises from −8° C. to +7° C.) whereupon most of the solid dissolves. After 30 min stirring at room temperature a white solid precipitated and the resulting mixture was then diluted with water and acidified with HCl (4 N). The white precipitate was then filtered off, washed with water and dried under high vacuum to afford the title compound (27.0 g, 97%) which was obtained as an off white solid. MS: m/e=155.1 [M]+.

Workup

  1. dissolutiondissolves
  2. customprecipitated
  3. additionthe resulting mixture was then diluted with water
  4. filtrationThe white precipitate was then filtered off
  5. washwashed with water
  6. customdried under high vacuum

Sources & evidence

ORD record
ord-e468646ae8604abcbcc3b948e63b9c2d
Source dataset
uspto-grants-2013_12
Patent number
US08604062B2

Reaction notes

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