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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52386Generated: October 29, 2026

Ethyl 6-chloronicotinate → Ethyl-6-[(2,2,4,4,7-pentamethyl-6-chromanyl)-ethynyl]nicotinate

https://huagongshe.com/reaction/52386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-chloronicotinateHCID 2799611—
Reactant2,2,4,4,7-Pentamethyl-6-ethynyl-chromanHCID 15661139—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
ProductEthyl-6-[(2,2,4,4,7-pentamethyl-6-chromanyl)-ethynyl]nicotinateHCID 15661156—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 300 mg (1.316 mmol) of 2,2,4,4,7-pentamethyl-6-ethynyl-chroman (Compound 48) and 245.6 mg (1.3276 mmol) of ethyl 6-chloro-nicotinate (Compound 29) in 2 ml of triethylamine was placed in a pressure tube and a stream of nitrogen was bubbled through the solution for 15 min. The tube was then flushed with argon and a finely ground mixture of 100 mg (0.1425 mmol) of bis (triphenylphosphine) palladium (II) chloride and 50 mg (0.2625 mmol) of cuprous iodide was added to the solution. The pressure tube was then sealed and the reaction mixture heated at 60 degrees C. for 72 h. The mixture was cooled to room temperature and the triethylamine removed under vacuum. The residue was purified by flash chromatography (silica; 10% ethyl acetate in hexane) to give the title compound as a yellow solid. PMR (CDCl3): & 1.37 (6H, s), 1.38 (6H, s), 1.44 (3H, t, J-7.2 Hz), 1.85 (2H, s), 2.49 (3H, s), 4.43 (2H, q, J-7.2 Hz), 6.70 (1H, s), 7.55-7.61 (2H, m), 8.28 (1H, dd, J-8.2 Hz, 2.1 Hz), 9.22 (1H, d, J-2.1 Hz). MS exact mass, m/e 377.1982 (calcd. for C24H27O3N, 377.1991).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616597
Source datasetuspto-grants-1997_04
ORD IDord-c99fb797ca1043db8b003e48950c84a9
Source noteuspto-grants-1997_04