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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018764Generated: October 27, 2026

2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol → 2,2,8,8-Tetramethylnona-3,6-diyn-5-one

https://huagongshe.com/reaction/1018764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,8,8-Tetramethyl-3,6-nonadiyn-5-olHCID 11355997—
CatalystNickel oxide (Ni2O3)HCID 10313272—
SolventBenzeneHCID 241—
Product2,2,8,8-Tetramethylnona-3,6-diyn-5-oneHCID 535094—

Reaction Conditions

Temperature7.5 °C

Reaction Steps

The 2,2,8,8-tetramethylnona-3,6-diyn-5-ol prepared in Part A (7.0 g, 36 mmole) was dissolved in 150 mL of benzene, cooled to 5-10° C. and nickel peroxide (18.15 g, 200 mmole) was added over a period of 20 minutes. After the addition had been completed, the reaction mixture was stirred at room temperature for 30 minutes, then filtered, and the nickel peroxide left on the filter was washed well with benzene and then with dichloromethane. The filtrate was evaporated to give a yellow solid, which was recrystallized from benzene to give 2,2,8,8-tetramethylnona-3,6-diyn-5-one as pale yellow crystals (4.2 g). The structure of this product was confirmed by fast atom bombardment (FAB) mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482950B1
Source datasetuspto-grants-2002_11
ORD IDord-969fe95dd5ec4ffe8d68ddd0da54b220
Source noteuspto-grants-2002_11