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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894999Generated: November 1, 2026

Acetic Acid → HCID 86737963, compound

https://huagongshe.com/reaction/894999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantButyl nitriteHCID 10996—
ReactantHCID 564736HCID 564736—
SolventWaterHCID 962—
ProductHCID 86737963HCID 86737963—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 21.0 g. (0.133 mole) of 4-(1-hydroxyethyl)-1-methyl-cyclohexene, 23 mg. glacial acetic acid and 26 ml. n-butylnitrite at 0° C. there is added dropwise a solution of 5 ml. concentrated hydrochloric acid and 5 ml. glacial acetic acid. After two additional hours while maintaining the temperature at 0° C., 500 ml. water is added and the solution is extracted with diethyl ether. These ether extracts are washed with water and brine and dried over magnesium sulfate. The magnesium sulfate is removed by filtration and the solution evaporated to give 2-chloro-5-(1-hydroxyethyl)-2-methyl-cyclohexanone oxime. To this compound is added 12.0 g. anhydrous sodium acetate and 50 ml. glacial acetic acid. This mixture is heated at 100° for one hour and poured into 250 ml. water. After sitting for several hours, the aqueous solution is extracted several times with ether and the combined ether extracts are washed with brine and sodium bicarbonate, dried over magnesium sulfate, filtered and evaporated to give 1,3-dimethyl-2-oxabicyclo[2,2,2]octan-6-one-oxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04285944
Source datasetuspto-grants-1981_08
ORD IDord-d74084d0fca04a7889d1481676a5beb6
Source noteuspto-grants-1981_08