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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464600Generated: October 30, 2026

Hydrochloric Acid → HCID 12097219, compound

https://huagongshe.com/reaction/1464600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
ReactantHCID 178418680HCID 178418680—
SolventDiethyl EtherHCID 3283—
ProductHCID 12097219HCID 1209721967.7%

Reaction Steps

8.63 g (0.05 mole) of 2-chloro-4'-fluoroacetophenone were dissolved in 60 ml of diethyl ether. The solution was stirred under a stream of nitrogen, and 200 ml (0.057 mole) of a diethyl ether solution of trimethylsilylmethylmagnesium chloride were added dropwise at such a rate that the temperature of the reaction mixture did not rise above 15° C.-20° C. The reaction mixture was then stirred for a further 1 hour at room temperature, after which it was poured into 200 ml of ice water, and its pH was adjusted to a value of 6-7 by the addition of 5% w/v aqueous hydrochloric acid. It was then extracted with 100 ml of ethyl acetate. The organic extract was washed twice, each time with 50 ml of a saturated aqueous solution of sodium chloride It was then dried over anhydrous sodium sulfate, and the solvent was removed by distillation under reduced pressure, to afford a crude oily product. This crude oily product was purified by silica gel column chromatography, using mixtures of ethyl acetate and hexane ranging from 1:10 to 1:5 by volume, to give 8.8 g (yield 67.7%) of the title compound as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306712
Source datasetuspto-grants-1994_04
ORD IDord-0746a5345041433a8ae27610ef50f37a
Source noteuspto-grants-1994_04