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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597898Generated: October 31, 2026

HCID 22503258, compound → HCID 67271323, compound

https://huagongshe.com/reaction/597898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22503258HCID 22503258—
ReactantHCID 178418361HCID 178418361—
CatalystLindlars catalystHCID 131709914—
SolventEthyl AcetateHCID 8857—
ProductHCID 67271323HCID 6727132349.1%

Reaction Steps

The 4-(5-bromo-pyridin-2-yl)-but-3-yn-2-ol prepared in Step 1 (2.26 g, 0.010 mol) was dissolved in EtOAc (50 mL). Lindlar's catalyst (1.13 g) was added and the mixture was shaken on a Parr shaker under 55 psi hydrogen for 16 h. The mixture was filtered and concentrated. The residue was chromatographed (SiO2, 9/1 to 4/1 hexane/EtOAc) to afford 4-(5-bromo-pyridin-2-yl)-but-3-en-2-ol as a clear oil (1.12 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897601B2
Source datasetuspto-grants-2011_03
ORD IDord-3d38aa97e027431fb010887885e13949
Source noteuspto-grants-2011_03