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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279484Generated: October 29, 2026

Toluene → HCID 53980081, compound

https://huagongshe.com/reaction/279484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantCysteamine HydrochlorideHCID 9082—
Reactant2-[(alpha-Methyl-3-trifluoromethylbenzylidene)aminooxy]-alpha-methoxyiminophenylacetaldehydeHCID 86584678—
Solvent1-ButanolHCID 263—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 53980081HCID 5398008196.7%

Reaction Steps

Toluene (2.5 ml), butanol (2.5 ml), cysteamine hydrochloride (0.29 g, 2.54 mmol) and triethylamine (0.26 g, 2.54 mmol) were added to 2-[(α-methyl-3-trifluoromethylbenzylidene)aminooxy]-α-methoxyiminophenylacetaldehyde (0.48 g, 1.27 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-[(α-methyl-3-trifluoromethylbenzylidene)aminooxy]phenyl thiazolidin-2-yl ketone O-methyloxime (0.52 g, yield 93.6%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-b050555b3fe74a179d8e7a6eedead1bb
Source noteuspto-grants-2002_03