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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 2,6-dichloropyridine-4-carboxylateHCID 22594123—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
CatalystCID 53485975HCID 53485975—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-chloro-6-vinylisonicotinateHCID 86657031—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598209B2
Source datasetuspto-grants-2013_12
ORD IDord-b1ef76f1dd724efba1104e1d847d998f
Source noteuspto-grants-2013_12