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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444264Generated: October 25, 2026

Isoamyl Nitrite → Methyl 2-hydroxyimino-2-(isothiazol-4-yl)acetate

https://huagongshe.com/reaction/444264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantSodiumHCID 5360545—
ReactantMethyl 2-(isothiazol-4-yl)acetateHCID 12906554—
SolventMethanolHCID 887—
ProductMethyl 2-hydroxyimino-2-(isothiazol-4-yl)acetateHCID 5731077261%

Reaction Steps

A solution of sodium (1.01 g.) in absolute methanol (10 ml.) was dropwise added over 15 minutes with stirring and ice-cooling to a solution of methyl 2-(isothiazol-4-yl)acetate (6.30 g.) and isopentyl nitrite (10.6 g.) in absolute methanol (63 ml.). The mixture was stirred for 30 minutes at the same temperature and for 3 hours at ambient temperature. The reaction mixture was concentrated and the residue was poured into a mixture of ethyl acetate (50 ml.) and water (50 ml.) The aqueous layer was separated and the ethyl acetate layer was extracted twice with 1 N aqueous solution of sodium hydroxide (20 ml. and 10 ml.). The extracts and the aqueous layer separated above were combined, adjusted to pH 1 with 10% hydrochloric acid and extracted twice with ethyl acetate (70 ml. and 50 ml.). The extracts were washed with a 5% aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give methyl 2-hydroxyimino-2-(isothiazol-4-yl)acetate (anti isomer) (4.55 g.), mp 110° to 112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04263291
Source datasetuspto-grants-1981_04
ORD IDord-3ae38d61da354f90a6929c50ae284757
Source noteuspto-grants-1981_04