ChemicalBook--->CAS DataBase List--->116047-26-8

116047-26-8

116047-26-8 Structure

116047-26-8 Structure
IdentificationBack Directory
[Name]

Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate
[CAS]

116047-26-8
[Synonyms]

7-methoxycarbonyl-1,2,3,4-tetrahydronaphthalene-1-one
methyl 8-oxo-6,7-dihydro-5H-naphthalene-2-carboxylate
methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate
Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate
2-Naphthalenecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-, methyl ester
[Molecular Formula]

C12H12O3
[MDL Number]

MFCD16037868
[MOL File]

116047-26-8.mol
[Molecular Weight]

204.22
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate(116047-26-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID

89781-52-2

Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate

116047-26-8

Intermediate VIII: Steps for the synthesis of methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate: Step a) Preparation of methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate: to a methanolic solution of 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid (16 g, 0.084 mol) was added sulfoxide chloride (23 g, 0.2 mol). The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate (200 mL), the organic layer was washed with 10% aqueous sodium bicarbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate 16 g (94% yield) as a liquid. Thin layer chromatography (TLC) conditions: chloroform/methanol (9/1, v/v), Rf = 0.9.

[References]

[1] Patent: WO2005/12280, 2005, A1. Location in patent: Page/Page column 55
[2] Helvetica Chimica Acta, 1993, vol. 76, # 4, p. 1539 - 1563
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