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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435274Generated: October 25, 2026

Propargyl bromide → Ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate

https://huagongshe.com/reaction/435274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetateHCID 6802348—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetateHCID 5412433577%

Reaction Steps

Propargyl bromide (4.16 g.) was added to a suspension of ethyl 2-(2-tritylaminothiazol-4-yl)-2-hydroxyiminoacetate (syn isomer, 10 g.), potassium carbonate (4.84 g.) and N,N-dimethylformamide (22 ml.) under atmosphere of nitrogen gas and stirred at room temperature for 100 minutes. The insoluble substance was filtered off and washed with a little of N,N-dimethylformamide. The filtrate and washing solution were combined together, and water (400 ml.) was added to the solution. After the suspension was extracted with ethyl acetate (400 ml.), the extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After treating the solution with activated charcoal, the solution was concentrated in vacuo. The residue was triturated with diisopropyl ether. The precipitates were collected by filtration, and washed with diisopropyl ether to give ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate (syn isomer, 8.34 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400379
Source datasetuspto-grants-1983_08
ORD IDord-5537b0307c7344c382a333f53719a103
Source noteuspto-grants-1983_08