HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → HCID 14856650, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- | HCID 11037 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14856647 | HCID 14856647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 14856650 | HCID 14856650 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250699 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-db261b774a6f427ab6c2689174032dc2 |
| Source note | uspto-grants-1993_10 |