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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479382Generated: November 1, 2026

Hydrochloric Acid → HCID 18770380, compound

https://huagongshe.com/reaction/479382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 18770424HCID 18770424—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 18770380HCID 1877038051%

Reaction Steps

The crude crystals (17.1 g) of di-tert-butyl 2,2-bis[(4-pyridyl)methyl]malonate synthesized by the above process were dissolved in trifluoroacetic acid (90 ml), and the solution was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the resultant concentrated residue was heated for 20 minutes in a bath controlled at 200° C. and then dissolved in methanol (170 ml). A 4N hydrogen chloride in ethyl acetate (100 ml; 400 mmol) was added to the solution, and the mixture was stirred for 2 hours and then concentrated under reduced pressure. The resultant concentrated residue was made basic by addition of aqueous 2.5N sodium hydroxide and extracted with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 6.0 g (yield: 51%) of methyl 2,2-bis[(4-pyridyl)methyl]acetate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645957B2
Source datasetuspto-grants-2003_11
ORD IDord-87b6fb6618a944bbaf6784355d3dfcf7
Source noteuspto-grants-2003_11