Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919053Generated: November 1, 2026

2-Bromonicotinaldehyde → 1-(2-Bromo-pyridin-3-yl)-4-phenyl-butan-1-ol

https://huagongshe.com/reaction/919053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromonicotinaldehydeHCID 4714951—
ReactantHCID 178418471HCID 178418471—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Bromo-pyridin-3-yl)-4-phenyl-butan-1-olHCID 86697088—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-pyridine-3-carbaldehyde (1.25 g, 6.72 mmol) was dissolved in THF (10 mL) and cooled to 0° C. 3-phenyl-propyl magnesium bromide (0.5 M in THF, 20.2 mL, 10.08 mmol) was slowly added and the reaction stirred at 0° C. for 1 hour and then at room temperature for 30 minutes. The reaction was monitored by TLC and when complete was quenched with 10 mL of NH4Cl (sat'd, aq.). The volume of THF was reduced and the reaction was submitted to EtOAc/H2O workup. The crude material was purified on silica gel (0-100% EtOAc in hexanes) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09272990B2
Source datasetuspto-grants-2016_03
ORD IDord-1c0a5ec6736c4bba97a1ba8ffb48b2a3
Source noteuspto-grants-2016_03