HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243537Generated: October 30, 2026
Pyridine → Tert-butyl 4-cyano-3,3-dimethylbutanoate
https://huagongshe.com/reaction/1243537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Tert-butyl 5-amino-3,3-dimethyl-5-oxopentanoate | HCID 21927924 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 4-cyano-3,3-dimethylbutanoate | HCID 21927900 | 72.4% |
Reaction Steps
Tert-butyl 5-amino-3,3-dimethyl-5-oxopentanoate (3.17 g, 14.7 mmol) was dissolved in dioxane (32 mL) containing pyridine (8 mL) and the solution was cooled to 0° C. Trifluoroacetic anhydride was added dropwise over 25 minutes keeping the temperature between 0–5° C. The mixture was stirred at 0° C. for one hour and then at room temperature overnight. A few chips of ice were added, followed by ethyl acetate (250 mL). The ethyl acetate was washed with brine, dried (Na2SO4) and removed under reduced pressure. The residue was purified by flash chromatography 7:3 (hexane:ethyl acetate) to give 2.1 g (72%) of the desired product. 1H NMR (CDCl3) 2.44 (s, 2H), 2.21 (s, 2H), 1.39 (s, 9H), 1.10 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119098B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-16986769068c4ed5abe69363c5da97f0 |
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| Source note | uspto-grants-2006_10 |
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