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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296007Generated: October 30, 2026

Hydrochloric Acid → HCID 53875379, compound

https://huagongshe.com/reaction/2296007

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 1 N 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-allyloxyimino-2-(2-formamido-5-chlorothiazol-4-yl)acetic acid (syn isomer) (24.74 g), mp. 166° to 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427677
Source datasetuspto-grants-1984_01
ORD IDord-9dc59a1a6f694ceeaa81df68a9b4f22c
Source noteuspto-grants-1984_01