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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274970Generated: November 2, 2026

Trityl chloride → ethyl (2Z)-2-[5-methyl-2-(tritylamino)-1,3-thiazol-4-yl]-2-trityloxyiminoacetate

https://huagongshe.com/reaction/1274970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantHCID 88197801HCID 88197801—
SolventEthyl AcetateHCID 8857—
Productethyl (2Z)-2-[5-methyl-2-(tritylamino)-1,3-thiazol-4-yl]-2-trityloxyiminoacetateHCID 8819838940.1%

Reaction Steps

To a suspension of sodium hydride (1.37 g) in 110 ml of ethyl acetate, ethyl 2-(5-methyl-2-tritylaminothiazol-4-yl)-2-(Z)-(hydroxyimino)acetate (16.15 g) was added at room temperature. The mixture was treated with a solution of trityl chloride (9.55 g) in ethyl acetate (66 ml). After 20 hours, the reaction was quenched by ice-water. The aqueous phase was extracted with ethyl acetate, and the combined extracts were washed with brine and dried with magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel with 5%-17% ethyl acetate/hexane to give 9.8 g of ethyl 2-(5-methyl-2-tritylaminothiazol-4-yl)-2-(Z)-(trityloxyimino)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159961
Source datasetuspto-grants-2000_12
ORD IDord-6acfca054a9e40fc9f2ca961ed659c21
Source noteuspto-grants-2000_12