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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027525Generated: November 4, 2026

Homoallyl bromide → HCID 178450298, compound

https://huagongshe.com/reaction/1027525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoallyl bromideHCID 21241—
ReactantHCID 57548087HCID 57548087—
ReactantHCID 178420268HCID 178420268—
SolventDiethyl EtherHCID 3283—
ProductHCID 178450298HCID 17845029843%

Reaction Steps

Compound 32D was prepared following the procedure as described for the synthesis of compound 32A (see Scheme 5) using 4-bromo-but-1-ene as the alkyl halogenide and 3-pyridin-3-yl-1-(2-trimethylsilanyl-1-ethoxymethyl)-1H-pyrazol-4-ol (30). Work-up and flash chromatography (diethyl ether) afforded compound 31D. Yield 43% (oil, TLC diethyl ether Rf 0.37), which was subsequently deprotected (TBAF/THF) to afford 3-(4-but-3-enyloxy-1H-pyrazol-3-yl)-pyridine (32D).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735388B2
Source datasetuspto-grants-2014_05
ORD IDord-988b8a9eb4b84e7eb9881d1cb49f6b5a
Source noteuspto-grants-2014_05