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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267814Generated: October 26, 2026

N-Methylformanilide → 4-(Cyclohex-1-EN-1-YL)benzaldehyde

https://huagongshe.com/reaction/267814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylformanilideHCID 66737—
Reactant1-Bromo-4-(cyclohex-1-en-1-yl)benzeneHCID 2326691—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product4-(Cyclohex-1-EN-1-YL)benzaldehydeHCID 23508852—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a solution of 7 g of p-(1-cyclohexenyl)-phenylbromide in 100 ml of absolute ether there is added at 5° C, while stirring and in an atmosphere of nitrogen, 50 ml of a solution of 4.3 g of n-butyl-lithium in absolute ether. The mixture is allowed to reach room temperature, stirred for 30 minutes at 30° C, then cooled to 20° C and a solution of 4 g of N-methyl-N-formyl-aniline in 50 ml of absolute ether is added dropwise, when the internal temperature rises to 30° C. After the reaction mixture has been allowed to continue to react for 30 minutes at room temperature, it is poured into 100 ml of ice cold 2N hydrochloric acid and extracted with ether. The ether layers are washed with water, dried over sodium sulphate and evaporated in vacuo. The residue is distilled under a high vacuum and yields the p-(1-cyclohexenyl)-benzaldehyde having a boiling point of 110°-120° C (0.2 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944589
Source datasetuspto-grants-1976_03
ORD IDord-552285c1844e457baa7ab28f95d0b375
Source noteuspto-grants-1976_03