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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387359Generated: October 31, 2026

Toluene → 2-(2,5-dimethylphenoxymethyl)phenyl thiazolidin-2-yl ketone O-methyloxime

https://huagongshe.com/reaction/1387359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantCysteamine HydrochlorideHCID 9082—
Reactant2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetaldehydeHCID 53861051—
Solvent1-ButanolHCID 263—
SolventSodium chloride; waterHCID 57417360—
Product2-(2,5-dimethylphenoxymethyl)phenyl thiazolidin-2-yl ketone O-methyloximeHCID 5453988191.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268312B1
Source datasetuspto-grants-2001_07
ORD IDord-3f37bb35794442a9b2e8dafa0a5b7931
Source noteuspto-grants-2001_07