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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074936Generated: October 27, 2026

Hydrochloric Acid → 2-(2-Cyclohexen-1-yl)oxyimino-2-(2-aminothiazol-4-yl)acetic acid

https://huagongshe.com/reaction/1074936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Thiazoleacetic acid, 2-amino-alpha-oxo-HCID 12783320—
Reactant(2-Formamido-1,3-thiazol-4-yl)(oxo)acetic acidHCID 13116693—
Reactant2-[(Cyclohex-2-en-1-yl)oxy]-1H-isoindole-1,3(2H)-dioneHCID 13577106—
Reactant(2-Cyclohexen-1-yl)oxyamine hydrochlorideHCID 20274566—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(2-Cyclohexen-1-yl)oxyimino-2-(2-aminothiazol-4-yl)acetic acidHCID 54291324—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of N-(2-cyclohexen-1-yl)oxyphthalimide (17.6 g) and hydrazine hydrate (7.2 g) in ethanol (180 ml) was stirred for 1.5 hours at 60° C. After the addition of water (100 ml) and conc.hydrochloric acid (20 ml) to the reaction mixture, the resulting mixture was filtered and the filtrate was evaporated. The remaining mixture was filtered to give the filtrate containing (2-cyclohexen-1-yl)oxyamine hydrochloride (Filtrate A). To a suspension of 2-(2-formamidothiazol-4-yl)glyoxylic acid (10.0 g) in water (50 ml) was added a solution of sodium hydroxide (4.4 g) in water (50 ml). The resulting mixture was stirred for 2.5 at room temperature and the mixture containing 2-(2-aminothiazol-4-yl)glyoxylic acid was adjusted to pH 7.0 with 10% hydrochloric acid and then thereto was added the above obtained Filtrate A. The mixture was stirred for 2 hours at room temperature. The reaction mixture was adjusted to pH 7.5 with 4 N aqueous solution of sodium hydroxide and then evaporated. The residue was washed with ethyl acetate and then adjusted to pH 2.0 with 10% hydrochloric acid. The precipitates were collected by filtration, washed with water, dried over phosphorus pentoxide to give 2-(2-cyclohexen-1-yl)oxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer) (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394384
Source datasetuspto-grants-1983_07
ORD IDord-150423d7501140099cc595f804a7d577
Source noteuspto-grants-1983_07