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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406367Generated: October 26, 2026

Methyl dichlorophosphate → 5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrile

https://huagongshe.com/reaction/406367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl dichlorophosphateHCID 69611—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amideHCID 66618802—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrileHCID 6661893979.6%

Reaction Steps

Methyl dichlorophosphate (1.9 mL) was added dropwise at 20° C. or less to an ice-cooled solution of 5-chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amide (3.0 g) and 1,8-diazabicyclo[5,4,0]undec-7-ene (6.4 mL) in methylene chloride (30 mL). After completion of the dropwise addition, the reaction solution was stirred at room temperature for one hour and 25 minutes. A saturated sodium bicarbonate aqueous solution was added to the reaction solution. After stirring for five minutes, the organic layer was separated. The aqueous layer was reextracted with methylene chloride. The combined organic layers were sequentially washed with 1 N hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Wakogel C-200; elution solvent:heptane:ethyl acetate=49:1→19:1) to obtain 2.25 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754100B2
Source datasetuspto-grants-2014_06
ORD IDord-a1c3ad42df04461db79b9e1cc1260091
Source noteuspto-grants-2014_06