Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 12961712 | HCID 12961712 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54165256 | HCID 54165256 | — |
Reaction Steps
1 g of [3-(4-chlorophenyl)-2-oxo-4-phenyl-4-imidazolin-1-yl] acetic acid are dissolved in a small amount of anhydrous chloroform. 0.7 g of thionylchloride are added thereto and the mixture is stirred at about 50° C. for 2 hours. The mixture is evaporated in a vacuum, the residue is mixed with a small amount of chloroform and 0.31 g of hexanol are added to the mixture. After stirring for one hour at room temperature, the CHCl3 -solution is first extracted with an NaHCO3 -solution and then with water. It finally is dried over Na2SO4. The CHCl3 -solution is evaporated, remaining hexanol is distilled off a high vacuum and the residue is further purified chromatographically on silicic acid gel using CHCl3 as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04349684 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-7d27a07bc68f40fb8e10d982a4e5de06 |
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| Source note | uspto-grants-1982_09 |
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