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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463916Generated: October 30, 2026

Thionyl Chloride → Ethyl 2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetate

https://huagongshe.com/reaction/463916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 2-methoxyimino-3-t-butoxycarbonylhydrazonobutyrateHCID 54569379—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetateHCID 53899707—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of ethyl 2-methoxyimino-3-t-butoxycarbonylhydrazonobutyrate (a mixture of syn and anti isomers) (28.7 g.) and thionyl chloride (30 ml.) was warmed with stirring on a water bath of 50° C. for 3 minutes and then stirred for 5 minutes at ambient temperature to give black solution. To the reaction mixture was added ethyl acetate (200 ml.) and the mixture was poured into ice-water (300 ml.). The ethyl acetate layer was separated, washed in turn with water, with a saturated aqueous solution of sodium bicarbonate and with a saturated aqueous solution of sodium chloride. After drying over magnesium sulfate, the ethyl acetate solution was treated with activated charcoal and concentrated to give black oil. The oil was purified by column chromatography on silica gel using a mixture of benzene and ethyl acetate (19:1) as an eluent to give ethyl 2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetate (anti isomer) (4 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544751
Source datasetuspto-grants-1985_10
ORD IDord-c9f9405f7b8d476faee61dc755163787
Source noteuspto-grants-1985_10