Hydroxylamine → Methyl 4-[amino(hydroxyimino)methyl]-2-methoxybenzoate

HRID 219846Notes

Reaction equation

[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([O:13][CH3:14])[CH:4]=1)#[N:2].[NH2:15][OH:16]>CCO>[NH2:2][C:1](=[N:15][OH:16])[C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([O:13][CH3:14])[CH:4]=1

Participants

Conditions

Temperature: 60 °C

Procedure

To a suspension of methyl 4-cyano-2-methoxybenzoate, obtained in step 1 (155 mg; 0.81 mmol; 1 eq.) in EtOH (1.55 mL) was added hydroxylamine (50% in water) (0.24 mL; 4.05 mmol; 5 eq.). The reaction mixture was stirred at 60° C. for 60 min. Solvents were removed to dryness, to afford the title compound as a yellow powder. 1H NMR (DMSO-d6, 400 MHz) δ 10.62 (br s, 1H), 9.85 (s, 1H), 7.64 (d, J=7.9 Hz, 1H), 7.40 (s, 1H), 7.35-7.31 (m, 2H), 5.95 (br s, 2H), 3.85 (s, 3H), 3.78 (s, 3H).

Workup

customSolvents were removed to dryness

Sources & evidence

ORD record: ord-5de15077b83b4b838e83385582869ad5
Source dataset: uspto-grants-2012_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08202865B2

Reaction notes

Loading…