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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620936Generated: October 31, 2026

Dimethylformamide → HCID 14477042, compound

https://huagongshe.com/reaction/620936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantOxalyl chlorideHCID 65578—
Reactant3,3,3-Trifluoro-2-phenylpropanoic acidHCID 287249—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 14477042HCID 14477042—

Reaction Steps

To a solution of 10 g of trifluoromethylphenylacetic acid (0.049 mole) dissolved in 100 ml dichloromethane and 0.5 ml dimethylformamide was added 8.9 g (0.07 mole) of oxalyl chloride dropwise over 1/2 hour. After the evolution of gases had ceased, the liquid was roto-evaporated. To the residue was added 5.75 g (0.049 mole) of zinc cyanide and approximately 100 ml of acetonitrile. The mixture was stirred for 15 minutes at room temperature, and then 5.5 g (0.49 mole) of 1,3-cyclohexanedione was added, followed by dropwise addition of 6.06 g (0.06 mole) of triethylamine. After the exothermic reaction had subsided, the mixture was then refluxed for one hour. Thereafter it was cooled to room temperature and the acetonitrile was removed in vacuo. To the residue was added 2N hydrochloric acid, and the mixture was extracted with ether, after which the organic layer was washed with 5% potassium carbonate. The aqueous layer was acidified and the product obtained which was 2.4 g of substance, identified by suitable analytical techniques as being the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822905
Source datasetuspto-grants-1989_04
ORD IDord-dcb10bffc03c43b486bdd3e4532d07f5
Source noteuspto-grants-1989_04