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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711517Generated: October 25, 2026

Triethylamine → HCID 68477280, compound

https://huagongshe.com/reaction/1711517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(S)-(+)-4-Penten-2-olHCID 6994332—
Reactant3-Bromo-5-(propan-2-yloxy)pyridineHCID 10584808—
CatalystTri-o-tolylphosphineHCID 80271—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductHCID 68477280HCID 6847728060.7%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 5-bromo-3-isopropoxypyridine (12.56 g, 58.13 mmol), (2S)-4-penten-2-ol (5.00 g, 58.05 mmol), palladium(II) acetate (130 mg, 0.58 mmol), tri-o-tolylphosphine (706 mg, 2.32 mmol), triethylamine (35 mL, 252 mmol) and acetonitrile (35 mL) was heated in a sealed glass tube at 130-140° C. for 8 h. The reaction mixture was cooled to ambient temperature. The solvent was removed under reduced pressure on a rotary evaporator. Water (50 mL) was added and the mixture was extracted with chloroform (3×50 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over silica gel, eluting with chloroform-acetone (95:5, v/v). Selected fractions were combined and concentrated by rotary evaporation, producing 7.80 g (60.7%) of a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790757B2
Source datasetuspto-grants-2010_09
ORD IDord-b699b6358e8549459cc964e968dd6a5d
Source noteuspto-grants-2010_09