Dimethylformamide → 3-(3,4-Difluorophenyl)prop-2-enoyl chloride

HRID 2404974Notes

Reaction equation

HRID 2404974 reaction equation
[C:1](Cl)(=O)[C:2]([Cl:4])=[O:3].[F:7][C:8]1[CH:9]=[C:10](/[CH:15]=C/C(O)=O)[CH:11]=[CH:12][C:13]=1[F:14].CN(C)C=O>ClCCl>[F:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:1][C:2]([Cl:4])=[O:3])[CH:11]=[CH:12][C:13]=1[F:14]

Participants

5

Procedure

At 0-5° C., oxalyl dichloride (25.7 g, 202.36 mmol, 3.00 equiv.) was added to a mixture of (E)-3-(3,4-difluorophenyl)acrylic acid (12.4 g, 67.38 mmol, 1.00 equiv.), N,N-dimethylformamide (1 mL), and dichloromethane (150 mL). The solution was stirred at ambient temperature for about 2 hours, and then concentrated in vacuo to give the title product, which was used in the next step without any further purification.

Workup

  1. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-409b3651cf8a466f9f5e41cc6c52b8b7
Source dataset
uspto-grants-2014_08
Patent number
US08802850B2

Reaction notes

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