4-Phenyl-3-butyn-2-one → HCID 178467506, compound
Reaction equation
[C:1]([C:4]#[C:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:3])[CH3:2].C[Si]([N:16]=[N+:17]=[N-:18])(C)C>CCOCC>[C:1]([C:4]1[N:16]=[N:17][NH:18][C:5]=1[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 140 °C
Procedure
A mixture of 30 g (0.21 mole) of acetylphenyl-acetylene and 24 g (0.21 mole) of trimethylsilyl azide was heated at 140°C for 24 hours. It was then cooled, dissolved in ether, and extracted with dilute sodium hydroxide. This aqueous layer was separated and made acidic with dilute HCl. The precipitate was recrystallized from benzene-petroleum ether to give 11 g (28%) of 4-acetyl-5-phenyltriazole, m.p. 117°-118°C.
Workup
- temperatureIt was then cooled
- extractionextracted with dilute sodium hydroxide
- customThis aqueous layer was separated
- customThe precipitate was recrystallized from benzene-petroleum ether
Sources & evidence
- ORD record
- ord-7ba1df873209404cb8b825f3a7b3368f
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03985765
Reaction notes
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