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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085205Generated: October 31, 2026

Allyl bromide → HCID 20061622, compound

https://huagongshe.com/reaction/1085205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl 2-oxo-4-(trifluoromethyl)-2,3-dihydro-1,3-thiazole-5-carboxylateHCID 2783041—
ReactantPotassiumHCID 5462222—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 20061622HCID 20061622—

Reaction Steps

10 g of ethyl 2,3-dihydro-2-oxo-4-trifluoromethyl-5-thiazolcarboxylate (CA Vol. 92 110 998P), 200 ml of toluene, 2.6 g of potassium in pastilles, 6 ml of allyl bromide and 2.8 g of tetrabutylammonium bromide were heated at 90° C. for 3 hours and the mixture was allowed to return to ambient temperature followed by stirring for 2 hours. The mixture was washed with a N sodium hydroxide solution, with a N hydrochloric acid solution, with water and with a saturated sodium chloride solution. Drying, filtering and concentrating were carried out and the residue was chromatographed on silica and eluted with a hexane-ethyl acetate mixture (9-1) to obtain 8.65 g of the expected product with a Rf=0.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008281
Source datasetuspto-grants-1991_04
ORD IDord-8711d457e6d8439ea6d610146b8b79cb
Source noteuspto-grants-1991_04