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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964907Generated: October 30, 2026

Acetic Acid → 1-Chloro-1,1-difluoro-5,5-dimethyl-2,4-hexanedione

https://huagongshe.com/reaction/964907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPinacoloneHCID 6416—
ReactantAcetic acid, 2-chloro-2,2-difluoro-, ethyl esterHCID 67843—
ReactantSodium MethoxideHCID 10942334—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Chloro-1,1-difluoro-5,5-dimethyl-2,4-hexanedioneHCID 1315961149%

Reaction Steps

7.1 g of sodium methoxide was added to 100 ml of dry ether, and the mixture was stirred. A solution of 20 g of ethyl chlorodifluoroacetate diluted with 25 ml of dry ether was added dropwise at room temperature. Further, a solution of 12.5 g of pinacolone diluted with 25 ml of dry ether was added dropwise, and the mixture was stirred overnight at room temperature. Then, to the reaction solution, a solution of 8.4 g of glacial acetic acid diluted with 100 ml of water and a solution of 23.6 g of copper (II) acetate dissolved in a proper amount of water were added dropwise successively. The dropwise addition was followed by stirring for about 10 minutes. Then, the ether was distilled off under reduced pressure and the solid mass was filtered off. After vacuum drying, 100 ml of 6N hydrochloric acid was added, and extraction with ethyl acetate was carried out. The ethyl acetate layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. Then, the residue was subjected to vacuum distillation to obtain 13 g of the desired product. (b.p. 54°-57° C./5 mmHg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773388
Source datasetuspto-grants-1998_06
ORD IDord-b5aec8a062734837b531272d9ee650b0
Source noteuspto-grants-1998_06