Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727879Generated: October 31, 2026

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

https://huagongshe.com/reaction/727879

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 4s) 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 numberUS05045551
Source datasetuspto-grants-1991_09
ORD IDord-ff98afd79feb4c0f9108a382a8e68e8b
Source noteuspto-grants-1991_09