Hydroxyamine hydrochloride → (NE)-N-[(5-bromo-2-fluoro-3-methylphenyl)methylidene]hydroxylamine

HRID 1502901Notes

Reaction equation

HRID 1502901 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([F:10])=[C:6]([CH:9]=1)[CH:7]=O.C([O-])(=O)C.[Na+].Cl.[NH2:18][OH:19]>C(O)C>[Br:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([F:10])=[C:6]([CH:9]=1)/[CH:7]=[N:18]/[OH:19]

Participants

5

Procedure

To a stirred solution of 5-bromo-2-fluoro-3-methylbenzaldehyde (3.5 g, 16.2 mmol) in ethanol (50.0 mL) were added sodium acetate (2.0 g, 24.3 mmol) and hydroxylamine hydrochloride (1.69 g, 24.3 mmol) at ambient temperature. The reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was concentrated on rotavapour to obtain crude compound, which was washed with water filtered and dried under vacuum to afford the title compound as a white solid: mp 126-127° C.; 1H NMR (400 MHz, CDCl3) δ 8.32 (s, 1H), 7.73 (d, J=2.4 Hz, 1H), 7.51 (s, 1H), 7.34 (d, J=2.4 Hz, 1H), 2.25 (s, 3H); ESIMS m/z 232.10 ([M+H]+).

Workup

  1. concentrationThe reaction mixture was concentrated on rotavapour
  2. customto obtain crude compound, which
  3. washwas washed with water
  4. filtrationfiltered
  5. customdried under vacuum

Sources & evidence

ORD record
ord-1b47a63b262d401b8c8ec81e2fbe580d
Source dataset
uspto-grants-2015_12
Patent number
US09211280B2

Reaction notes

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