Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207893Generated: November 2, 2026

Thionyl Chloride → 3-(5-Bromo-pyridin-3-yl)-acryloyl chloride

https://huagongshe.com/reaction/2207893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(5-Bromopyridin-3-yl)prop-2-enoic acidHCID 2784735—
Product3-(5-Bromo-pyridin-3-yl)-acryloyl chlorideHCID 131735945—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-(5-Bromo-pyridin-3-yl)-acrylic acid (26.2 g, 114.7 mmol) prepared in Step 1 was added to thionyl chloride (100.0 mL). The reaction mixture was stirred at 100° C. for 2 hours and then concentrated under reduced pressure. The resulting residue was concentrated under reduced pressure three times, along with using toluene, to give 3-(5-bromo-pyridin-3-yl)-acryloyl chloride as an unpurified dark brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-01fe754c286948e4b62d352405604faf
Source noteuspto-grants-2016_06