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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393813Generated: October 28, 2026

Dimethylformamide → HCID 178516667, compound

https://huagongshe.com/reaction/2393813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactant2'-Fluoro-6'-(trifluoromethyl)acetophenoneHCID 519414—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 178516667HCID 178516667—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 2'-fluoro-6'-(trifluoro-methyl)acetophenone (3.0 g, 14.5 mmol), carbon disulfide (1.5 mL, 26.7 mmol) and dimethylformamide (DMF) (12.5 mL) in benzene at 15°-25° C. is treated portion-wise with a 60% dispersion of sodium hydride in mineral oil (1.15 g, 28.8 mmol NaH) over a 1.5 hour period, stirred for 0.5 hour, heated at 125° C. for 1 hour, cooled to room temperature and diluted with water. The resultant mixture is treated with acetic acid and extracted with ether. The aqueous phase is acidified to pH 3 with HCl and extracted with ethyl acetate. The ethyl acetate extracts are combined, washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo to give an orange oil residue. The residue is crystallized from diethyl ether/hexanes to give the title product as a white solid, 3.0 g (79% y), mp 142°-144° C., identified by IR, 1HNMR, 19FNMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05808105
Source datasetuspto-grants-1998_09
ORD IDord-2c66ae4510b1450083b6ad5006de25a0
Source noteuspto-grants-1998_09