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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484468Generated: October 26, 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/484468

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 Steps

The 2,2,8,8-tetramethyl-nona-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, 465 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-tetramethyl-nona-3,6-diyn-5-one as pale yellow crystals (4.2 g). The structure of this product was confirmed by FAB mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231190
Source datasetuspto-grants-1993_07
ORD IDord-f4cc986354bf4aa49bf8aaa9abefbd1b
Source noteuspto-grants-1993_07