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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650615Generated: October 25, 2026

4-Piperidinone, 3,5-dibromo-2,2,6,6-tetramethyl-, hydrobromide (1:1) → 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxylic Acid (5-Hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)-amide

https://huagongshe.com/reaction/1650615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinone, 3,5-dibromo-2,2,6,6-tetramethyl-, hydrobromide (1:1)HCID 89251—
Reactant6-Amino-2,2-dimethyl-1,3-dioxepan-5-olHCID 3387444—
ReactantPotassium tert-butoxideHCID 23665647—
SolventIsopropanolHCID 3776—
Product2,2,5,5-Tetramethyl-3-pyrroline-3-carboxylic Acid (5-Hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)-amideHCID 54204802—

Reaction Steps

Analogously to Example 7, 78.79 g (200 mmol) of 3,5-dibromo-2,2,6,6-tetramethylpiperidin-4-one hydrobromide, 69.34 g of potassium tert-butylate, and 35.47 g (220 mmol) of 6-amino-2,2-dimethyl-1,3-dioxepan-5-ol are reacted in 800 ml of isopropanol and then extracted with dichloromethane. Yield: 37.66 g (60.3% of theory) of 2,2,5,5-tetramethyl-3-pyrroline-3-carboxylic acid (5-hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)amide which, crystallized from diethyl ether/hexane, shows a melting point of 125°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925652
Source datasetuspto-grants-1990_05
ORD IDord-68ec87766cf24c4886b2a9ee93ed4117
Source noteuspto-grants-1990_05