Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657580Generated: October 31, 2026

Carbon Tetrachloride → 5-Chloro-2-methoxy-3-pyridinecarbonyl chloride

https://huagongshe.com/reaction/1657580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Chloro-2-methoxynicotinic acidHCID 9836973—
SolventBenzeneHCID 241—
Product5-Chloro-2-methoxy-3-pyridinecarbonyl chlorideHCID 20156610—

Reaction Steps

To a suspension of 3.76 g. (0.02 mole) of 5-chloro-2-methoxynicotinic acid in 100 ml. of carbon tetrachloride, there were added 100 ml. of thionyl chloride in one portion and the resulting mixture was then refluxed on a steam bath for a period of 90 minutes. Upon completion of this step, the clear solution so obtained was cooled and then concentrated in vacuo at room temperature to afford a residual oil. The excess thionyl chloride present was next removed in the same manner as described in Preparation A for the production of 2-methoxynicotinoyl chloride, except that only 100 ml. of benzene was employed this time (i.e., during each purification step). The yield of pure 5-chloro-2-methoxynicotinoyl chloride, obtained as the residual product, was quantitative in this particular instance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03961065
Source datasetuspto-grants-1976_06
ORD IDord-da49a25e91114e4d8907dd163c963add
Source noteuspto-grants-1976_06