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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897823Generated: November 1, 2026

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

https://huagongshe.com/reaction/1897823

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 numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-77267cc8a10949439a0ac554ef006c9e
Source noteuspto-grants-2013_08