4-Fluorobenzaldehyde → 4-Fluoro-benzaldehyde O-methyl-oxime

HRID 1836460Notes

Reaction equation

HRID 1836460 reaction equation
Cl.[O:2]([NH2:4])[CH3:3].C([O-])(=O)C.[Na+].[F:10][C:11]1[CH:18]=[CH:17][C:14]([CH:15]=O)=[CH:13][CH:12]=1>O.O1CCCC1.CCOCC>[CH3:3][O:2][N:4]=[CH:15][C:14]1[CH:17]=[CH:18][C:11]([F:10])=[CH:12][CH:13]=1

Participants

7

Reactant 3

HCID 680234-FluorobenzaldehydeHCID 517045Sodium AcetateHCID 521874O-Methylhydroxylamine hydrochloride

Product 1

HCID 539632384-Fluoro-benzaldehyde O-methyl-oximeYield 100.2%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
22 °C

Procedure

A solution of methoxylamine hydrochloride (13.4 g, 0.16 mol) in a mixture of water (150 ml) and tetrahydrofuran (50 ml) was treated with sodium acetate (11.2 g, 0.136 mol) followed by 4-fluorobenzaldehyde (11.57 g, 93.2 mmol) and the resulting mixture was stirred at 22° C. for 4 hours. The reaction mixture was then diluted with ether, washed with brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave 14.3 g of the crude title material as a clear oil which was used as such for the next step. Distillation of an aliquot in vacuo gave a clear oil; bp 45-50° C./0.5 torr. 1HNMR 400 MHz (CDCl3) δ (ppm): 3.99 (3H, s), 7.09 (2H, m), 7.6 (2H, m), 8.06 (1H, s).

Workup

  1. washwashed with brine
  2. dry with materialdried over anhydrous magnesium sulfate
  3. customEvaporation of the solvent under reduced pressure

Sources & evidence

ORD record
ord-0e5e0ec2fdf1487f8ff957d696b47078
Source dataset
uspto-grants-2004_08
Patent number
US06777440B2

Reaction notes

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