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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168416Generated: November 2, 2026

4-Chlorobenzyl cyanide → HCID 69976413, compound

https://huagongshe.com/reaction/1168416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzyl cyanideHCID 241582—
ReactantBenzoic acid, 2-(trifluoromethyl)-, ethyl esterHCID 521815—
ReactantSodium ethoxideHCID 2723922—
SolventTolueneHCID 1140—
ProductHCID 69976413HCID 6997641350.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624179B1
Source datasetuspto-grants-2003_09
ORD IDord-a8c7a45f5c16410eb7a494ff35233fb2
Source noteuspto-grants-2003_09