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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250142Generated: October 25, 2026

Acetoacetic Acid → Acetoacetic Acid

https://huagongshe.com/reaction/250142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoacetic AcidHCID 96—
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductAcetoacetic AcidHCID 96—
Product5-Ethyl-2-pyridineethanolHCID 78894—

Reaction Steps

Bromination of olefin 2 with bromine in a neutral solvent e.g. dichloromethane, carbon tetrachloride, can give 5. Similarly, cyclic sulfate 10a may be prepared via oxidation of cyclic sulfite 10b, which in turn may be obtained form diol 11 by reacting with thionyl chloride, in the presence of bases e.g. pyridine, triethylamine. The formation of diol 11, can be achieved from diacetate 17, by treatment with base in water or methanol or ethanol. Alternatively, one can also prepare diol 11, from the diacetate 17 which in turn can be obtained from N-oxide of 5-ethyl-2-pyridyl-2-ethanol as shown in scheme I. In an the above transformations (Scheme I) upon completion of the reaction, the desired compound is easily isolated from the reaction mixture in a most conventional manner eg. extracting in organic layer, washing with water, drying organic layer, concentrating and purifying/crystallizing the desired final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863300B2
Source datasetuspto-grants-2011_01
ORD IDord-f59aabf097bb4a138279ddd1f834b118
Source noteuspto-grants-2011_01