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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845290Generated: October 31, 2026

1,3-Benzenedicarboxylic acid, 5-bromo-, 1,3-dimethyl ester → HCID 58188082, compound

https://huagongshe.com/reaction/1845290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzenedicarboxylic acid, 5-bromo-, 1,3-dimethyl esterHCID 103954—
Reactant5-Methyl-2-(tri-n-butylstannyl)pyridineHCID 11132711—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 58188082HCID 58188082—

Reaction Steps

A mixture of dimethyl 5-bromoisophthalate (1.0 g, 3.66 mmol), 5-methyl-2-(tributylstannyl)pyridine (1.5 mL, 4.5 mmol), tetrakis(triphenylphosphine)palladium(0) (200 mg, 0.17 mmol), and toluene (10 mL) under nitrogen was subjected to microwave irradiation at 120° C. for 2 hour. The mixture was cooled to room temperature and the precipitate was collected via filtration and rinsed with hexane to afford a white solid which was the desired product. The filtrate was purified via flash chromatography to afford another crop of the desired product (0.8 g in total). LC-MS: 286.3 [M+1]+; 1H NMR (400 MHz, CDCl3): 8.84 (d, J=1.6 Hz, 2H), 8.71 (t, J=1.6 Hz, 1H), 8.56 (t, J=0.8 Hz, 1H), 7.75 (d, J=8.0 Hz, 1H), 7.61 (dd, J=2.0, 8.1 Hz, 1H), 3.98 (s, 6H), 2.41 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-7b848cb7091d44fe90d866d988478c3d
Source noteuspto-grants-2015_02