HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909133Generated: October 30, 2026
Triethylamine → tert-Butyl 2-chloro-6-vinylisonicotinate
https://huagongshe.com/reaction/1909133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl 2,6-dichloropyridine-4-carboxylate | HCID 22594123 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 2-chloro-6-vinylisonicotinate | HCID 86657031 | — |
Reaction Steps
To a solution of tert-butyl 2,6-dichloroisonicotinate (11.0 g, 44.3 mmol) in THF (200 mL) were added potassium vinyltrifluoroborate (7.1 g, 53.2 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.97 g, 1.33 mmol) and triethylamine (9.3 mL, 66.5 mmol). The mixture was heated to 65° C. After 1 h, saturated aqueous sodium bicarbonate was added and the mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→90% hexanes/ethyl acetate) gave no separation of desired product. The mixture was carried onto next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598209B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-b1ef76f1dd724efba1104e1d847d998f |
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| Source note | uspto-grants-2013_12 |
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