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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380081Generated: November 1, 2026

Toluene → o-Nitrophenyl cyclopropyl ketone

https://huagongshe.com/reaction/2380081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-2'-nitrobutyrophenoneHCID 11806412—
SolventWaterHCID 962—
Producto-Nitrophenyl cyclopropyl ketoneHCID 1048794723.6%

Reaction Steps

The 13.8% toluene solution of 4-chloro-2'-nitrobutyrophenone obtained in Example 6 is treated, with stirring, first with 90 mL water and second with 50% NaOH (48 g, 0.6 mole NaOH). The resultant reaction mixture is allowed to exotherm, then is heated at 85°-90° C. for 2-3 hours, cooled to room temperature and allowed to settle. The phases are separated and the organic phase is washed with water. The aqueous phases are combined and washed with toluene. The organic phases are combined and concentrated in vacuo to give the title product as a toluene solution, 235 g, 23.6% title product by LC analysis (91% yield from furanone). The product solution is used as is in Example 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364968
Source datasetuspto-grants-1994_11
ORD IDord-e5ce432022d24f8abe3808ece7c815d0
Source noteuspto-grants-1994_11