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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397023Generated: October 27, 2026

Potassium Acetate → 2,2-bis(fluoromethyl)-6-trifluoromethyl-2H-1-benzopyran-4-carboxylic acid

https://huagongshe.com/reaction/397023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactanttrifluoromethanesulfonic acid 2,2-bis(fluoromethyl)-6-(trifluoromethyl)-2H-1-benzopyran-4-yl esterHCID 12070531—
ReactantHCID 178418416HCID 178418416—
SolventDimethylacetamideHCID 31374—
Product2,2-bis(fluoromethyl)-6-trifluoromethyl-2H-1-benzopyran-4-carboxylic acidHCID 9879640—

Reaction Steps

A three-necked 50-ml flask (equipped with a reflux condenser, a thermometer, and a CO introducing pipe connected with a balloon charged with carbon monoxide gas) was charged with 1.0 g (2.4 mmol) of trifluoromethanesulfonic acid 2,2-bis(fluoromethyl)-6-(trifluoromethyl) -2 H- 1-benzopyran-4-yl ester, 0.95 g (9.7 mmol) of potassium acetate, and 10 ml of N,N-dimethylacetamide. Under stirring of the mixture, predetermined amounts of reagents were added, as shown in Table. Then, the reaction was conducted under conditions shown in Table. After that, the reaction mixture was subjected to the same post-treatments as those of Example 5. As a result, 2,2-bis(fluoromethyl)-6-(trifluoromethyl)-2 H- 1-benzopyran-4-carboxylic acid was obtained, as shown by yield in Table.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608217B2
Source datasetuspto-grants-2003_08
ORD IDord-b3fa476485b843eb8e67422a2e199b84
Source noteuspto-grants-2003_08