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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366137Generated: November 2, 2026

Dimethylformamide → 1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride

https://huagongshe.com/reaction/2366137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidHCID 22250323—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chlorideHCID 22250333—

Reaction Steps

A sample of crude 1-phenyl-3-(trifluoromethyl)pyrazole-5-carboxylic acid (i.e. the product of Step B) (4.13 g, 16.1 mmol) was dissolved in methylene chloride (45 mL). The solution was treated with oxalyl chloride (1.80 mL, 20.6 mmol), followed by N,N-dimethylformamide (0.010 mL, 0.13 mmol). Off-gassing began shortly after adding the N,N-dimethylformamide catalyst. The reaction mixture was stirred for ˜20 minutes under ambient conditions, then was heated to reflux for a period of 35 minutes. Volatiles were removed by stripping the reaction mixture on a rotary evaporator at a bath temperature of 55° C. The product consisted of 4.43 g of a light-yellow oil. The only imparity observed by 1H NMR was N,N-dimethylformamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697734B2
Source datasetuspto-grants-2014_04
ORD IDord-3cb4044ed24c4945a66a94b0b0568b35
Source noteuspto-grants-2014_04