HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 4-[6-(2,3-Dimethoxyphenyl)hexyloxy]-3-propylbenzoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(6-Bromohexyl)-2,3-dimethoxybenzene | HCID 14986283 | — |
| Reactant | Ethyl 4-hydroxy-3-propylbenzoate | HCID 14986319 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-[6-(2,3-Dimethoxyphenyl)hexyloxy]-3-propylbenzoic acid ethyl ester | HCID 14986320 | 97.2% |
Reaction Steps
A mixture of 1.40 g (4.8 mmol) of 1-(6-bromohexyl)-2,3-dimethoxybenzene, 1.00 g (4.8 mmol) of 4-hydroxy-3-propylbenzoic acid ethyl ester, 1.30 g (9.6 mmol) of potassium carbonate and 0.72 g (4.8 mmol) of sodium iodide in 35 mL of acetone was stirred at reflux for 47 hours. Workup and purification as described in Example 16 gave 2.0 g of 4-[6-(2,3-dimethoxyphenyl)hexyloxy]-3-propylbenzoic acid ethyl ester as an oil. The mass spectrum showed the molecular ion at m/e 428.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05191108 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-e002763901344fc08e45656d420fdf58 |
| Source note | uspto-grants-1993_03 |