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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069504Generated: October 30, 2026

Pyridine → HCID 58198422, compound

https://huagongshe.com/reaction/2069504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantHCID 87247012HCID 87247012—
SolventDimethylformamideHCID 6228—
ProductHCID 58198422HCID 58198422—

Reaction Conditions

Temperature50 °C

Reaction Steps

The crude 6-chloro-pyridine-3-sulfinic acid sodium salt (4.7 mmol) was suspended in DMF (20 mL). Pyridine (0.8 mL) and ethyl α-bromoisobutyrate (1 mL) were added. The reaction was stirred at 50° C. under nitrogen for 18 h. The reaction mixture was partitioned between diethyl ether (100 mL) and water (50 mL). The organic layer was washed with brine (50 mL) and dried over Na2SO4. Filtration, concentration under reduced pressure, followed by column chromatography (silica, eluent heptanes, 0-25% ethyl acetate) afforded 0.83 g of 2-(6-chloro-pyridine-3-sulfonyl)-2-methyl-propionic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299111B2
Source datasetuspto-grants-2012_10
ORD IDord-6bd14382a100403cbf8ba2ef75fbecc2
Source noteuspto-grants-2012_10