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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709175Generated: October 30, 2026

p-Anisoyl chloride → HCID 53674212, compound

https://huagongshe.com/reaction/1709175

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 15696557HCID 15696557—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 53674212HCID 53674212—

Reaction Steps

11.2 cm3 of a 1.6M solution of n-butyllithium in n-hexane is added at -40° C. to a solution, cooled to -45° C., of 2.8 g of 5-n-butyloxy pyrrolidin-2-one in 70 cm3 of tetrahydrofuran with agitation for 30 minutes. Under the same conditions, a solution of 5.24 g of anisoyl chloride (at 58% in toluene) in 6 cm3 of tetrahydrofuran is added. After agitation for 2 hours, allowing to return to ambient temperature, the mixture is evaporated to dryness. The oil obtained is chromato-graphed on silica (eluent: toluene-ethyl acetate 8-2) and 2 g of the product sought is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948804
Source datasetuspto-grants-1990_08
ORD IDord-eea80835df834b3aba75ae0044836063
Source noteuspto-grants-1990_08