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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027969Generated: November 1, 2026

Hydrochloric Acid → HCID 59637316, compound

https://huagongshe.com/reaction/1027969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantEthyl chlorophenylacetateHCID 97752—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59637316HCID 5963731644.9%

Reaction Conditions

Temperature-45 °C

Reaction Steps

9.8 g of potassium tert-butylate were dissolved in 90 mL of DMF and cooled to −45° C. To this, a mixture of ethyl 2-chloro-2-phenylacetate (43.8 mmol, 8.7 g) and 1-fluoro-2-nitrobenzene (43.8 mmol, 4.6 mL) was gently added dropwise and stirring was continued for a further 20 minutes. The reaction mixture was set to pH 4 with aq. 16% strength. HCl, diluted with 25 mL of water, and extracted with EA (3×50 mL). Following combination of the organic phases, they were washed with water and sat. aq. NaCl solution, dried over MgSO4 and concentrated in vacuo. The resulting residue was purified by column chromatography (silica gel: mesh 100-200, eluent: 10% EA in cyclohexane) and yielded 5.9 g (44.9%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735426B2
Source datasetuspto-grants-2014_05
ORD IDord-4aa9740996db4975bc4e04773757726e
Source noteuspto-grants-2014_05