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ChemicalBook--->CAS DataBase List--->89691-88-3

89691-88-3

89691-88-3 Structure

89691-88-3 Structure
IdentificationBack Directory
[Name]

5,7-Diaza-spiro[3.4]octane-6,8-dione
[CAS]

89691-88-3
[Synonyms]

NSC 51773
5,7-Diaza-spiro[3.4]octane-6,8-dione
5,7-Diaza-Spiro[3.4]Octane-6,8-Dione(WX619040)
[Molecular Formula]

C6H8N2O2
[MOL File]

89691-88-3.mol
[Molecular Weight]

140.14
Chemical PropertiesBack Directory
[Melting point ]

224 - 225°C
[density ]

1.39±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

10.46±0.20(Predicted)
[color ]

White to Off-White
Spectrum DetailBack Directory
[Spectrum Detail]

5,7-Diaza-spiro[3.4]octane-6,8-dione (89691-88-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

sodium:cyanide

773837-37-9

Cyclobutanone

1191-95-3

Ammonium carbonate

506-87-6

5,7-Diaza-spiro[3.4]octane-6,8-dione

89691-88-3

34 General procedure for the synthesis of 5,7-diazaspiro[3.4]octane-6,8-dione from the compound (CAS: 773837-37-9), cyclobutanone and ammonium carbonate: 34.1 Sodium cyanide (1.47 g, 30 mmol) and ammonium carbonate (7.5 g, 78 mmol) were added to the reaction flask under argon protection. Subsequently, a mixed ethanol-water solvent (16 mL) solution of cyclobutanone (1.49 mL, 20 mmol) was added to the reaction system at 23°C. The reaction mixture was heated to 70 °C with continuous stirring for 6 hours. Upon completion of the reaction, the reaction mixture was cooled, poured into water (15 mL), and then concentrated hydrochloric acid (13 mL) solution was slowly added. Stirring was continued at 23 °C for 10 hours. After that, ethanol and some water were removed from the reaction mixture using a rotary evaporator. The precipitate was filtered through a glass filter and washed with distilled water. The target compound 5,7-diazaspiro[3.4]octane-6,8-dione was finally obtained as a beige powder in 39% yield (1.1 g). 1H NMR (400 MHz, DMSO-d6) δ: 10.49 (s, 1H, NH), 8.27 (s, 1H, NH), 2.31-2.37 (m, 2H, CH2), 2.19-2.27 (m, 2H, CH2), 1.83-1.90 (m, 1H, CHA), 1.71-1.76 (m, 1H, CHB ). Melting point: 223-225°C.

[References]

[1] Patent: US2012/83514, 2012, A1. Location in patent: Page/Page column 19
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