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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655623Generated: November 3, 2026

Sulfuric Acid → HCID 14856650, compound

https://huagongshe.com/reaction/1655623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBenzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 14856647HCID 14856647—
SolventEthanolHCID 702—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 14856650HCID 1485665085%

Reaction Steps

A mixture of 2.12 g (4 RS, 5 R)-1,3-dibenzyl-2-oxo-5-(4-oxo-4-phenyl-2-thiabutyl)imidazolidin-4-ol (prepared according to Example 3) and 100 ml of ethanol is brought to pH 3.1 (against Methyl Orange) at 0°-5° C. using 2 normal sulfuric acid in ethanol. After stirring at 0°-5° C. for two hours, the mixture is brought to pH 5 to 6 using 2% potassium hydroxide in ethanol. After customary working-up and flash chromatography, 2.043 g (91% of theory) of (4 RS, 5 R)-1,3-dibenzyl-2-oxo-5-(4-oxo-4-phenyl-2-thiabutyl)-4-ethoxyimidazolidine, Rf =0.69 (EtOAc/hexane 3:7), are obtained. The following are oxo-7-(methoxycarbonyl)-2-thiaheptyl)-4-ethoxyimidazolidine, yield 85% of theory, Rf =0.62 (EtOAc/hexane 1:1),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250699
Source datasetuspto-grants-1993_10
ORD IDord-db261b774a6f427ab6c2689174032dc2
Source noteuspto-grants-1993_10