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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608394Generated: October 31, 2026

Carbon Tetrachloride → HCID 14877939, compound

https://huagongshe.com/reaction/1608394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium AzideHCID 33557—
ReactantHCID 14877937HCID 14877937—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
ProductHCID 14877939HCID 1487793969.4%

Reaction Steps

To a suspension of 5.8 g (14 mmoles) of ethyl 3,3-bis-(4-fluorophenyl)-2-(benzoylamino)-2-propenoate and 11.2 g of triphenylphosphine in 150 mL of dry acetonitrile at room temperature was added dropwise 8.3 mL of carbon tetrachloride. The pale suspension was stirred for 45 minutes. To this clear orange solution was added 2.8 g of sodium azide and 1 g of tetra n-butyl ammonium bromide and stirring was continued. The orange suspension soon became pale with the formation of a white precipitate. After three hours, the mixture was filtered and the solution was concentrated under reduced pressure. More triphenylphosphine oxide was removed and the desired product was purified by crystallizations from ethyl acetate-hexanes to give 4.2 g (69%) of the title compound; m.p.=148.6-150.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870187
Source datasetuspto-grants-1989_09
ORD IDord-cbc441439fc14b85988987250bf6d565
Source noteuspto-grants-1989_09