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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650917Generated: November 3, 2026

Hydrochloric Acid → HCID 53875379, compound

https://huagongshe.com/reaction/1650917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantO-AllylhydroxylamineHCID 420841—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl (2-formamido-5-chlorothiazol-4-yl)glyoxylateHCID 14326717—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53875379HCID 5387537956.1%

Reaction Steps

Ethyl (2-formamido-5-chlorothiazol-4-yl)glyoxylate (40.0 g) was added to 1N aqueous solution of potassium hydroxide (305 ml) at ambient temperature and stirred for 10 minutes. The reaction mixture was adjusted to pH 2.0 with 10% aqueous hydrochloric acid under ice cooling. A solution of allyloxyamine (14.4 g) in tetrahydrofuran (200 ml) was added to the stirred suspension of the above mixture in pyridine (54.1 g) at ambient temperature and stirred for 4 hours at the same temperature. The resultant mixture was adjusted to pH 7.5 with a saturated aqueous solution of sodium bicarbonate, and washed with ethyl acetate. The separated aqueous layer was adjusted to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. The residue was washed with diisopropyl ether and collected by filtration to give 2-(2-formamido-5-chlorothiazol-4-yl)-2-allyloxyiminoacetic acid (syn isomer, 24.74 g), mp. 166° to 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925948
Source datasetuspto-grants-1990_05
ORD IDord-860f46bc43764c6a88888f7a006e15dc
Source noteuspto-grants-1990_05