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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693063Generated: November 2, 2026

Triethylamine → HCID 57458159, compound

https://huagongshe.com/reaction/1693063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantToluene ethylacetateHCID 21584019—
ReactantHCID 53420556HCID 53420556—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 57458159HCID 5745815994%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-6-tert-butylnaphthalene (980 mg, 3.72 mmol), palladium acetate (84 mg, 0.37 mmol), 1,3-bis(diphenylphophino)propane (153 mg, 0.37 mmol) and triethylamine (1.56 ml, 11.2 mmol) in MeOH (6 ml) and DMF (10 ml) was heated at 80° C. under carbon monooxide gas pressure (balloon) for 15 hours. After cooling to ambient temperature, the mixture was diluted with EtOAc-toluene (8:1) (160 ml) and filtered through a pad of celite. The filtrate and washings were washed with water, then brine, dried over sodium sulfate and evaporated in vacuo to give the crude product which was purified through silica gel column chromatography, eluting with hexane/EtOAc (10:1), to furnish the title compound as colorless oil (843 mg, 94%). 1H NMR (CDCl3): δ 1.43 (9H, s), 3.97 (3H, s), 7.61-7.67 (1H, m), 7.79-7.93 (3H, m), 8.01-8.07 (1H, m), 8.57 (1H, br, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158650B2
Source datasetuspto-grants-2012_04
ORD IDord-0e02d6c3793c496b90a381135fd19ef6
Source noteuspto-grants-2012_04