HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-(2,5-dimethylphenoxymethyl)phenyl thiazolidin-2-yl ketone O-methyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | 2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetaldehyde | HCID 53861051 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(2,5-dimethylphenoxymethyl)phenyl thiazolidin-2-yl ketone O-methyloxime | HCID 54539881 | 91.6% |
Reaction Steps
Toluene (3 ml), butanol (3 ml), cysteamine hydrochloride (0.34 g, 3.0 mmol) and triethylamine (0.42 ml, 3 mmol) were added to 2-(2,5-dimethylphenoxymethyl)-α-methoxyiminophenylacetoaldehyde (0.45 g, 1.5 mmol), and the mixture was stirred at room temperature for 1 hour. After completion of the reaction, half-saturated brine (100 ml) was added, and the mixture was extracted with dichloromethane (50 ml) twice. The extracts were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 2-(2,5-dimethylphenoxymethyl)phenyl thiazolidin-2-yl ketone O-methyloxime (0.49 g, yield 91.6%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362212B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-12feeacc00cb4ee69d69d0d3972d2727 |
| Source note | uspto-grants-2002_03 |