Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261987Generated: November 1, 2026

Water → Ethyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetate

https://huagongshe.com/reaction/261987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetateHCID 6802348—
SolventDimethylformamideHCID 6228—
SolventIsopropyl iodideHCID 6362—
ProductEthyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetateHCID 54071115—

Reaction Steps

A mixture of 6.86 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetate of Example 14, 3.51 g of potassium carbonate in 15 ml of dimethylformamide and 7.7 ml of isopropyl iodide was held under an argon atmosphere and stirring for 41/2 hours and then 250 ml of distilled water and 150 ml of ethyl acetate were added thereto with stirring. The mixture was decanted and the aqueous phase was washed with water and was extracted with ethyl acetate. The organic phase was dried, vacuum filtered and evaporated to dryness. The residue was taken up in ethanol and crystallization stated after seeding. The mixture was vacuum filtered and the precipitate was rinsed with ethanol and empasted with petroleum ether to obtain 3.26 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetate melting at 182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152432
Source datasetuspto-grants-1979_05
ORD IDord-2d7b8f48d33e48589412fcfdeb01e75a
Source noteuspto-grants-1979_05