Reaktion #1313

ord-37e5f74403034441b8cb09beed7ae702

Reaktionsgleichung

C#Cc1ccc2c(c1)C(C)(C)CCC2=O
6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
C#Cc1ccc2c(c1)C(C)(C)CCC2=O
Compound K
C#Cc1ccc2c(c1)C(C)(C)CCC2=O
6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1-one
CC1(C)CCC(=O)c2cc(Br)ccc21
Compound G
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1-one
C#Cc1ccc2c(c1)C(=O)CCC2(C)C
title compound
C#Cc1ccc2c(c1)C(=O)CCC2(C)C
7-Ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Employing the same general procedure as for the preparation of 6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound K), 7 g (27.6 mmol) of 7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound G) was converted into the title compound using 39 ml (36.6 mmol) of trimethylsilyl acetylene, 0.97 g (1.3 mmol) of bis(triphenylphosphine)palladium(II) chloride, 0.26 g (1.3 mmol) of cuprous iodide and 0.6 g (4.3 mmol) of K2CO3.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723620uspto-grants-1998_03