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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168415Generated: October 30, 2026

2-(Trifluoromethyl)benzoyl chloride → HCID 69976413, compound

https://huagongshe.com/reaction/1168415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactant4-Chlorobenzyl cyanideHCID 241582—
ReactantPotassiumHCID 5462222—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69976413HCID 6997641391.2%

Reaction Steps

A mixture comprising 45 g of 4-chlorobenzyl cyanide, 62 g of 2-trifluoromethylbenzoyl chloride and 210 ml of tetrahydrofuran, was dropwise added over a period of 1 hour at a temperature of not higher than 15° C. to the mixture comprising 70 g of potassium tertiary butyrate and 450 ml of tetrahydrofuran. After completion of the dropwise addition, the solution temperature was returned to room temperature, followed by the reaction for 1 hour. 500 ml of ice water was poured into the residue obtained by concentration under reduced pressure of the reaction mixture, followed by stirring for 15 minutes, whereupon the mixture was washed with 500 ml of methylene chloride. The aqueous layer was adjusted to pH 3 to 4 by concentrated hydrochloric acid and then extracted with 600 ml of methylene chloride. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. 300 ml of n-hexane was added to the residue, followed by washing to obtain 87.6 g of the desired product. The NMR spectrum data of this product are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624179B1
Source datasetuspto-grants-2003_09
ORD IDord-8a3cc9b4a0a748aa8e1538e1cd979108
Source noteuspto-grants-2003_09