![](/CAS/GIF/529-34-0.gif)
1-Tetralone synthesis
- Product Name:1-Tetralone
- CAS Number:529-34-0
- Molecular formula:C10H10O
- Molecular Weight:146.19
![Spiro[1,3-dithiane-2,1'(2'H)-naphthalene], 3',4'-dihydro-](/CAS/20210305/GIF/56685-73-5.gif)
56685-73-5
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![1-Tetralone](/CAS/GIF/529-34-0.gif)
529-34-0
478 suppliers
$6.00/10g
Yield:529-34-0 100%
Reaction Conditions:
with dihydrogen peroxide;tantalum pentachloride;sodium iodide in water;ethyl acetate at 20; for 0.3 h;
Steps:
6.2. General procedure for the deprotection of dithioacetals catalyzed by NaI-TaCl5
General procedure: A mixture of 1 (1.0 mmol), tantalum chloride (35.8 mg, 0.10 mmol), sodium iodide (15.0 mg, 0.10 mmol), and 30% hydrogen peroxide (0.46 ml, 4.0 mmol) in ethyl acetate (6 ml) and water (6 ml) was stirred at room temperature. The reaction was monitored by thin layer chromatography (TLC). After 1 disappeared on TLC, saturated aqueous sodium thiosulfate (4 ml), and saturated aqueous sodium bicarbonate (4 ml) were added to the reaction mixture. The organic layer was separated and the aqueous phase was extracted with ethyl acetate (25 ml×3). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate, and evaporated. Chromatography on silica gel gave a pure product.
References:
Kirihara, Masayuki;Noguchi, Takuya;Okajima, Nobuhiro;Naito, Sayuri;Ishizuka, Yuki;Harano, Aiko;Tsukiji, Hiroyuki;Takizawa, Ryu [Tetrahedron,2012,vol. 68,# 5,p. 1515 - 1520] Location in patent:experimental part
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529-34-0
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529-34-0
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![1-Tetralone](/CAS/GIF/529-34-0.gif)
529-34-0
478 suppliers
$6.00/10g
![1,2,3,4-Tetrahydro-1-naphthol](/CAS/GIF/529-33-9.gif)
529-33-9
193 suppliers
$6.00/250mg
![1-Tetralone](/CAS/GIF/529-34-0.gif)
529-34-0
478 suppliers
$6.00/10g