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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164602Generated: November 3, 2026

Sodium Hydroxide → HCID 12902718, compound

https://huagongshe.com/reaction/2164602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMonoperoxyphthalic acidHCID 75329—
ReactantHCID 12902717HCID 12902717—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 12902718HCID 12902718—

Reaction Conditions

Temperature10 °C

Reaction Steps

269 ml of a 0.09M solution of monoperphthalic acid in ether (prepared according VOGEL--Textbook of Practical Organic Chemistry, 1978, 307) are added rapidly to a solution of 7.9 g of 6-methoxy-4-[2-(1-benzoyl-4-piperidyl)-ethyl]-quinoline in 45 ml of methanol, stirred and cooled to 10° C. After four hours at the ambient temperature, a further 20 ml of the same monoperphthalic acid solution are added, and the stirring is then maintained for 15 hours. The reaction mixture is then made alkaline with 100 ml of a 0.7N aqueous solution of sodium hydroxide. The organic phase, separated, is again washed with 100 ml of a 0.5N solution of sodium hydroxide, dried, then concentrated. The residue obtained, after recrystallization from cyclohexane, gives 5.1 g of 6-methoxy-4-[2-(1-benzoyl-4-piperidyl)-ethyl]quinoline-N-oxide melting at 138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505916
Source datasetuspto-grants-1985_03
ORD IDord-5084a42e29c444c985bd74991d0eeea8
Source noteuspto-grants-1985_03