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893724-10-2

893724-10-2 Structure

893724-10-2 Structure
IdentificationBack Directory
[Name]

3-Oxo-cyclobutane-1,1-dic...
[CAS]

893724-10-2
[Synonyms]

3-Oxo-cyclobutane-1,1-dic...
Diisopropyl 3-oxocyclobutane-1,1-dicaboxylate
Diisopropyl 3-oxocyclobutane-1,1-dicarboxylate
dipropan-2-yl 3-oxocyclobutane-1,1-dicarboxylate
1,1-bis(propan-2-yl) 3-oxocyclobutane-1,1-dicarboxylate
3-Oxo-cyclobutane-1,1-dicarboxylic acid diisopropyl ester
1,1-Cyclobutanedicarboxylic acid, 3-oxo-, 1,1-bis(1-methylethyl) ester
[Molecular Formula]

C12H18O5
[MDL Number]

MFCD06742778
[MOL File]

893724-10-2.mol
[Molecular Weight]

242.27
Chemical PropertiesBack Directory
[Boiling point ]

293.2±40.0 °C(Predicted)
[density ]

1.165±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P280-P261
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Oxo-cyclobutane-1,1-dic...(893724-10-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Diisopropyl 3,3-dimethoxycyclobutane-1,1-dicarboxylate

115118-68-8

1,1-Cyclobutanedicarboxylic acid, 3-oxo-, 1,1-bis(1-methylethyl) ester

893724-10-2

General procedure for the synthesis of diisopropyl 3-oxocyclobutane-1,1-dicarboxylate from diisopropyl 3,3-dimethoxycyclobutane-1,1-dicarboxylate: in a round-bottomed flask containing a solution of 3,3-dimethoxycyclobutane-1,1-dicarboxylic acid diisopropyl 3,3-dimethoxycyclobutane-1,1-dicarboxylate (1.5 g, 5.20 mmol) in dichloromethane (20 mL), trifluoroacetic acid (2 mL, 26.0 mmol). The reaction mixture was stirred at room temperature for 2.5 hours. After the reaction was completed, the reaction mixture was diluted with ethyl acetate. The organic phase was washed sequentially with water, saturated sodium bicarbonate solution and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated to give diisopropyl 3-oxocyclobutane-1,1-dicarboxylate (1.2 g). The product was characterized by 1H NMR (400 MHz, CDCl3): δ 5.13 (dt, J = 12.5, 6.3 Hz, 2H), 3.64-3.53 (m, 4H), 1.32-1.24 (m, 12H).

[References]

[1] Synlett, 2009, # 11, p. 1827 - 1829
[2] Synlett, 2014, vol. 25, # 3, p. 355 - 358
[3] RSC Advances, 2016, vol. 6, # 27, p. 22737 - 22748
[4] Patent: US2009/233903, 2009, A1. Location in patent: Page/Page column 52
[5] Patent: WO2015/5901, 2015, A1. Location in patent: Page/Page column 702
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