Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297641Generated: October 29, 2026

Diisopropylamine → HCID 86752140, compound

https://huagongshe.com/reaction/2297641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantHCID 86752141HCID 86752141—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86752140HCID 8675214068.2%

Reaction Steps

Cool diisopropylamine dissolved in THF (60 mL) to 0-5° C. Add n-butyl lithium(39 mL, 97.99 mmol.) and stir the reaction at that temperature for 30 min. Canulate this reaction mixture to a cooled solution of N-(1,1-dimethylethyl)-2-bromo-3-methyl pyridine carboxamide (9.91 g, 97.99 mmol) in dry THF (250 mL) (−70° C.). Stir for 0.5 h then add 3-chlorobenzyl bromide(11.4 g, 55.31 mmol) dissolved in 50 mL of THF. Stir the reaction mixture for 0.5 h. Quench the reaction with water and extract the products twice with EtOAc. Dry the organic phase over Na2SO4, filter and chromatograph on silica gel column eluting with 3% MeOH solution in CH2Cl2 to give the title compound (15 g, Yield 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492381B1
Source datasetuspto-grants-2002_12
ORD IDord-ffd3561cd5d249668b5d127f93359ee3
Source noteuspto-grants-2002_12