Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407451Generated: October 30, 2026

5-Bromo-3-pyridinecarboxaldehyde → N-((5-bromopyridin-3-yl)methylene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/2407451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
ReactantTert-ButanesulfinamideHCID 3382465—
CatalystTitanium isopropoxideHCID 11026—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductN-((5-bromopyridin-3-yl)methylene)-2-methylpropane-2-sulfinamideHCID 66745079—

Reaction Steps

A mixture of 5-bromo-pyridine-3-carbaldehyde (2 g, 10.75 mmol), 2-methylpropane-2-sulfinamide (1.434 g, 11.83 mmol) and titanium(IV) isopropoxide (12.60 ml, 43.0 mmol) in toluene (53.8 ml) was stirred for 16 h at room temperature. Brine was added and the precipitate removed and washed with AcOEt. The organic layer was dried over MgSO4, filtered and concentrated to give the title compound that was used as is for the next step. LC-MS (M+1) 291.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809545B2
Source datasetuspto-grants-2014_08
ORD IDord-8976f4378e88476cb2170f4d099ef0ce
Source noteuspto-grants-2014_08