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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004383Generated: November 1, 2026

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

https://huagongshe.com/reaction/1004383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantTolueneHCID 1140—
ReactantCysteamine HydrochlorideHCID 9082—
Reactant2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetaldehydeHCID 53861051—
SolventTriethylamineHCID 8471—
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 =mol) 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 numberUS06048885
Source datasetuspto-grants-2000_04
ORD IDord-1cdf6cd10fdd4b43a1699ed27e5b4bf2
Source noteuspto-grants-2000_04