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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846231Generated: November 1, 2026

Triphenylphosphine → HCID 89964226, compound

https://huagongshe.com/reaction/1846231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 89964234HCID 89964234—
ReactantHCID 131732431HCID 131732431—
Catalystpalladium(II) acetateHCID 167845—
CatalystTetraethylammonium chloride monohydrateHCID 16211205—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 89964226HCID 89964226—

Reaction Conditions

Temperature110 °C

Reaction Steps

tert-butyl 9-methylene-6,7,8,9-tetrahydro-5H-pyrido[3,2-b]azepine-5-carboxylate. To a solution of tert-butyl (2-bromopyridin-3-yl)(pent-4-en-1-yl)carbamate (1 eq.) in DMF (0.2 M), PPh3 (0.25 eq.), Pd(OAc)2 (0.1 eq), and KOAc (5 eq.), is added, under an argon atmosphere, tetraethyl ammonium chloride hydrate (2 eq.). The flask is purged with argon for 15 min, and the resulting reaction mixture is stirred at 110° C. for 16 h. The reaction progress is monitored by TLC. The reaction mixture is diluted with EtOAc and saturated NaHCO3 solution. The organic layer is separated, dried over Na2SO4, and concentrated. The product thus obtained is purified by column chromatography to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952009B2
Source datasetuspto-grants-2015_02
ORD IDord-420a84676b5d47399ef8060f3b93ec9c
Source noteuspto-grants-2015_02