HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214541Generated: October 30, 2026
4-Fluorobenzaldehyde → 4-Fluoro-benzaldehyde O-methyl-oxime
https://huagongshe.com/reaction/2214541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Fluoro-benzaldehyde O-methyl-oxime | HCID 53963238 | 100.2% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07109186B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-b7f06f77d3fc48cba9644174433f1db1 |
|---|
| Source note | uspto-grants-2006_09 |
|---|