HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 12340623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(1H-Pyrrol-1-Yl)Phenol | HCID 712334 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 12340623 | HCID 12340623 | — |
Reaction Steps
p-Toluenesulfonic acid monohydrate (110 mg) is dissolved in 70 ml of dry benzene and the solution heated at reflux with a water-separator for about 10 minutes. A solution of 1-(o-hydroxyphenyl)-pyrrole (1.1 g) in dry benzene (80 ml) is added, followed by 10 ml of acetone. The reaction mixture is heated at reflux with the water-separator for 15 hr, cooled, and washed with a solution of NaHCO3. The benzene solution is evaporated to dryness. The residue is subjected to chromatography on silica gel, using chloroform as eluent. Evaporation of the first portion of the eluate gives the title compound, m.p. 38° - '° C, νmaxCHCl3 1600, 1510, 1345 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035495 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-30164572fc744f6e8990d6f64883ea67 |
| Source note | uspto-grants-1977_07 |