HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 4-Benzyloxy-7-(2-[4-fluorophenyl]ethoxy)coumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorophenethyl bromide | HCID 573153 | — |
| Reactant | 4-Benzyloxy-7-hydroxycoumarin | HCID 13408407 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-7-(2-[4-fluorophenyl]ethoxy)coumarin | HCID 22751306 | — |
Reaction Steps
A mixture of 4-benzyloxy-7-hydroxycoumarin (5.36; 0.02 mole) anhydrous potassium carbonate (4.0g) and 1-bromo-2-(4-fluorophenyl) ethane (4.06g) in acetone (100ml) was stirred at reflux for 20 hours and the inorganic material filtered off. Evaporation of the filtrate in vacuo gave an oil which rapidly set solid on scratching. Chloroform (200ml) was added and the mixture filtered to remove unchanged 4-benzyloxy-7-hydroxycoumarin. Reevaporation of the filtrate afforded a white solid, 3.34g (43%) of m.p. 120°,νmax (mull) 1715, 1675, 1620cm-1 ; τ(CDCl3); 6.93 (2H, t, J 6.7Hz); 5.80 (2H, t, J 6.7Hz); 4.87 (2H,S); 4.38 (1H,); 3.29-2.49 (6H, m) 2.32 (1H, d, J 10Hz); (Found C, 73.75 H,5.14 C24H19FO4 requires; C, 73.84; H, 4.91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04136192 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-9f9facb95fe340dbb588efe901358512 |
| Source note | uspto-grants-1979_01 |