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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168409Generated: November 2, 2026

Propyl chloroformate → HCID 70026627, compound

https://huagongshe.com/reaction/1168409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl chloroformateHCID 7998—
ReactantSodium hydrideHCID 24758—
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactant(4-tert-Butylphenyl)acetonitrileHCID 76784—
SolventDimethylformamideHCID 6228—
ProductHCID 70026627HCID 7002662769.9%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture comprising 2.0 g of 4-tert-butylbenzyl cyanide, 2.35 g of 2-trifluoromethylbenzoyl chloride and 8 ml of dimethylformamide, was dropwise added to a mixture comprising 0.84 g of 68% sodium hydride and 13 ml of dimethylformamide while maintaining the temperature at a level of from 40 to 50° C. After completion of the dropwise addition, the reaction was carried out for 30 minutes at room temperature. The reaction mixture was cooled with ice, and a mixture comprising 1.5 g of n-propyl chloroformate and 1.2 ml of dimethylformamide, was dropwise added. After completion of the dropwise addition, the reaction was carried out for 30 minutes under cooling with ice. The reaction mixture was poured into ice water and extracted with methylene chloride and then washed with water. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate/n-hexane=1/9) to obtain 3.4 g of the desired product (isomer ratio 7:93) having a melting point of 44 to 45° C. The HPLC conditions for the analysis of this product were the same as in Preparation Example 1. Further, 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-c111c1c2c91347a987b4e65564d01e3c
Source noteuspto-grants-2003_09