Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528757Generated: October 29, 2026

2-Bromopyridine → HCID 67979508, compound

https://huagongshe.com/reaction/528757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantTert-butyl 3-formylazetidine-1-carboxylateHCID 10726182—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 67979508HCID 67979508—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 1.51 g (9.55 mmol) bromopyridine in 50 mL ether at −20° C. was added 6 mL (1.6 M in hexane, 9.6 mmol) n-butyl lithium, after 10 minutes the mixture was cooled to −78° C. and 1.61 g (8.7 mmol) 3-formyl-azetidine-1-carboxylic acid tert-butyl ester in 20 mL ether was added. The mixture was stirred and allowed to warm to room temperature, quenched with 50 mL 1 M sodium bicarbonate solution and then extracted with 50 mL DCM. The organic layer was dried over Na2SO4. After filtration and evaporation of the solvent the desired product was purified by column chromatography (silica, heptane/EtOAc 1:1 to EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-4bce992c89684a5caac9563dac6b595a
Source noteuspto-grants-2016_05