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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64675Generated: October 29, 2026

Acetic Anhydride → HCID 178418479, compound

https://huagongshe.com/reaction/64675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant1-Oxo-1lambda~5~-pyridine-2,5-dicarboxylic acidHCID 13643503—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 178418479HCID 17841847979.1%

Reaction Steps

20.4 g of acetic acid anhydride (0.2 mole), 20.2 g of Et3N (0.2 mole) and 50 ml of CCl4 were put up in a flask. 18.3 g of isocinchomeronic acid-N-oxide (0.1 mole) was added by portions to this solution. The temperature rose to 50° C. After completion of the reaction the solvents were distilled off. About 100 ml of 20 percent KOH was added drop by drop to the viscous residue and the acetate was saponified over a 15 minute period at 80° C. After removal of the Et3N by extraction, the aqueous solution was acidified with concentrated HCl. The precipitate was sucked off, washed with water and dried under a vacuum. 11.0 g of 6-hydroxy nicotinic acid was obtained, which was pure according to NMR. The crude yield was about 79 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609734
Source datasetuspto-grants-1986_09
ORD IDord-52e57b3012044058a486db30d64d6456
Source noteuspto-grants-1986_09