HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Methylhydroxylamine hydrochloride → HCID 136127060, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | methyl E-2-(2-hydroxyphenyl)-2-methoxyimino-acetate | HCID 135424589 | — |
| Reactant | HCID 135703866 | HCID 135703866 | — |
| Reactant | HCID 178516824 | HCID 178516824 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136127060 | HCID 136127060 | — |
Reaction Steps
8.2 g (0.05 mol) of benzofuran-2,3-dione 2-oxime and 9 g (0.108 mol) of O-methylhydroxylamine hydrochloride in 50 ml of methanol are heated under reflux for 3 hours. The methanol is distilled off under reduced pressure and the residue is mixed with 50 ml of water and extracted with ethyl acetate. The organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure, giving 9.88 g of crystal-containing crude product. According to HPLC, the crude product contains 43.7% of methyl E-2-(2-hydroxyphenyl)-2-methoxyimino-acetate of log p=1.48 and 29.4% of methyl Z-2-(2-hydroxyphenyl)-2-methoxyimino-acetate of log p=2.37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660872B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-4315cc39b10b4d7ea0f723b6ad7ee611 |
| Source note | uspto-grants-2003_12 |