HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725713Generated: October 27, 2026
Hydrochloric Acid → HCID 18915764, compound
https://huagongshe.com/reaction/725713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanone, phenyl(2,4,6-trihydroxyphenyl)- | HCID 77093 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 18915764 | HCID 18915764 | 72.3% |
Reaction Steps
A mixture of 4.5 g (20 mmol) of 2,4,6-trihydroxybenzophenone, 9.8 g (40 mmol) of 1-bromododecane, 2.7 g (20 mmol) of potassium carbonate and 30 mg (0.2 mmol) of potassium iodide in 50 ml of toluene and 20 ml of N,N-dimethylacetamide is stirred at 110° C. for 7 h. The reaction mixture is cooled and then neutralized with 10% HCl. The organic solution is washed with water and then with saturated sodium chloride solution. The residue which remains after drying over MgSO4, filtering and concentrating by evaporation is purified by chromatography over silica gel (toluene/hexane 3:2). The product is recrystallized from isopropyl alcohol. 4.1 g of the compound are obtained as pale yellow crystals having a melting point of 37°-38° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05707690 |
|---|
| Source dataset | uspto-grants-1998_01 |
|---|
| ORD ID | ord-b5f895745b984e6d8f1230917c94552b |
|---|
| Source note | uspto-grants-1998_01 |
|---|