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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736409Generated: October 30, 2026

1,2-Dichloroethane → 161190-38-1

https://huagongshe.com/reaction/1736409

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHCID 10668289HCID 10668289—
ReactantCumen hydroperoxideHCID 53627471—
CatalystTitanium isopropoxideHCID 11026—
SolventWaterHCID 962—
Product161190-38-1HCID 98662153.2%

Reaction Conditions

Temperature-5 °C

Reaction Steps

To 1 l of 1,2-dichloroethane were added 56.8 g of titanium tetraisopropoxide, 168 g of D-(-)-diethyl tartarate, 0.91 ml of water and 80 g of 6-{3-[1-(2-methylphenyl)-2-imidazolylthio]propoxy}-3,4-dihydrocarbostyril. The mixture was stirred and then cooled to -5° C. Thereto was added 124 g of cumene hydroperoxide slowly. After the completion of the addition, the mixture was stirred at 5° C. for 18 hours. The reaction was repeated. The reaction mixtures from the two reactions were combined and purified by a silica gel column chromatography (eluant: dichloromethane/ethyl acetate/methanol=3/1/0→30/10/1), followed by recrystallization from ethanol-ethyl acetate. The mother liquor was concentrated to obtain crystals. This procedure was conducted 14 times. The resulting crystals were purified by a silica gel column chromatography (eluant: dichloromethane/ethyl acetate/methanol=30/10/1), followed by recrystallization from ethanol to obtain 2.7 g of (S)-(+)-6-{3-[1-(2-methylphenyl)-2-imidazolylsulfinyl]propoxy}-3,4-dihydrocarbostyril. White powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541198
Source datasetuspto-grants-1996_07
ORD IDord-7f2171dc27c749a5acd016514f343fd8
Source noteuspto-grants-1996_07