HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620936Generated: October 31, 2026
Dimethylformamide → HCID 14477042, compound
https://huagongshe.com/reaction/620936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3,3,3-Trifluoro-2-phenylpropanoic acid | HCID 287249 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14477042 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822905 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-dcb10bffc03c43b486bdd3e4532d07f5 |
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| Source note | uspto-grants-1989_04 |
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