HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 15676628, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 15676627 | HCID 15676627 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15676628 | HCID 15676628 | 55% |
Reaction Steps
A solution of thiophenol, sodium salt and methanol is added to a solution of 2-(1-benzoyl-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-(bromomethyl)nicotinic acid, methyl ester (14.08 g, 0.0298 mol) and methanol. The reaction mixture is stirred for 15 hours at room temperature, acidified with ammonium chloride (5 g, 0.0869 mol) and concentrated in vacuo to yield an oil. The oil is chromatographed using silica gel and hexanes/ethyl acetate (3:1) to (1:1) as eluant to give the title compound as a yellow solid (8.32 g, 55%), mp 135°-138° C., identified by IR and NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405827 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-31011027753b4e3eb594ee71acd7f0c6 |
| Source note | uspto-grants-1995_04 |