HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzyl cyanide → HCID 69976413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzyl cyanide | HCID 241582 | — |
| Reactant | Benzoic acid, 2-(trifluoromethyl)-, ethyl ester | HCID 521815 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69976413 | HCID 69976413 | 50.9% |
Reaction Steps
5.8 g of 4-chlorobenzyl cyanide, 10 g of ethyl 2-trifluoromethylbenzoate and 2.9 g of sodium ethylate were added to 100 ml of toluene and then reacted for 8 hours under reflux. The reaction mixture was returned to room temperature and extracted by an addition of 200 ml of water. The aqueous phase was adjusted to pH 6 to 7 with 6N hydrochloric acid and then extracted by an addition of 400 ml of methylene chloride. The organic layer was washed with water and a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 6.3 g of the desired product. The NMR spectrum data of this product were the same as in Reference Preparation Example 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06624179B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-a8c7a45f5c16410eb7a494ff35233fb2 |
| Source note | uspto-grants-2003_09 |