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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449058Generated: November 4, 2026

Sodium Hydroxide → 1-[(10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-yl)methyl]-4-piperidinone oxime

https://huagongshe.com/reaction/1449058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant1-[(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)methyl]-4-piperidinoneHCID 12515651—
SolventWater ethanolHCID 19096565—
Product1-[(10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-yl)methyl]-4-piperidinone oximeHCID 20375056—

Reaction Steps

2.6 Parts of finely ground sodium hydroxide is added to a suspension of 3 parts of 1-[(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)methyl]-4-piperidinone and 1.5 part of hydroxylamine hydrochloride in 50 parts by volume of ethanol-water (4:1) solution. The resultant mixture is heated on a steam bath for about 5 hours and then partitioned between water and ethyl acetate. The aqueous layer is separated and extracted with a second portion of ethyl acetate. The ethyl acetate extracts are combined, dried, and concentrated to give 1-[(10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-yl)methyl]-4-piperidinone oxime, as a white solid which melts at about 199°-202° C. after recrystallization from dioxane. This compound is represented by the following structural formula ##STR33##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188485
Source datasetuspto-grants-1980_02
ORD IDord-f6f5f6b918784c2e8c719673ddeb769d
Source noteuspto-grants-1980_02