HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479382Generated: November 1, 2026
Hydrochloric Acid → HCID 18770380, compound
https://huagongshe.com/reaction/479382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 18770424 | HCID 18770424 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 18770380 | HCID 18770380 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645957B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-87b6fb6618a944bbaf6784355d3dfcf7 |
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| Source note | uspto-grants-2003_11 |
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