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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703692Generated: October 30, 2026

Propargyl bromide → HCID 14695612, compound

https://huagongshe.com/reaction/703692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 14695585HCID 14695585—
SolventAcetonitrileHCID 6342—
ProductHCID 14695612HCID 1469561265%

Reaction Steps

To an acetonitrile solution (30 ml) of 3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (0.72 g, 2.5 mmol) was added sodium carbonate (0.16 g), and the mixture was heated at reflux for 1 hour. After the addition of propargyl bromide (0.36 g, 3.0 mmol), the reaction mixture was further refluxed for 1 hour. After the solution was quenched with 0.1N hdyrochloric acid, the product was extracted with chloroform. The extracts combined were dried and evaporated as small a volume as possible. The resulting pale yellow oil was purified by silica gel column chromatography to give pure 3-(2'-fluoro-4'-chloro-5'-propargyloxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione. (0.53 g, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983751
Source datasetuspto-grants-1991_01
ORD IDord-6eac2ddc3eb24808b337153d5d775f9c
Source noteuspto-grants-1991_01