| Identification | More | [Name]
Diethyl 1,1-cyclobutanedicarboxylate | [CAS]
3779-29-1 | [Synonyms]
1,1-CYCLOBUTANEDICARBOXYLIC ACID DIETHYL ESTER
1,1-DICARBOETHOXYCYCLOBUTANE
AKOS BBS-00006459
CYCLOBUTANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER
CYCLOBUTANE-1,1-DICARBOXYLIC ACID DIMETHYL ESTER
DIETHYL 1,1-CYCLOBUTANEDICARBOXYLATE
DIETHYL 2,2-TRIMETHYLENEMALONATE
DIETHYL CYCLOBUTANE-1,1-DICARBOXYLATE | [EINECS(EC#)]
223-239-4 | [Molecular Formula]
C10H16O4 | [MDL Number]
MFCD00019261 | [Molecular Weight]
200.23 | [MOL File]
3779-29-1.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H227 | [Precautionary statements ]
P210e-P280a-P370+P378a-P501a-P210-P280-P370+P378-P403+P235-P501 | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [REACH Registrations]
Active | [HS Code ]
38220090 | [Storage Class]
10 - Combustible liquids |
| Hazard Information | Back Directory | [Chemical Properties]
Colourless Oil | [Uses]
Intermediate in the production of Carboplatin | [Preparation]
The preparation of diethyl 1,1-cyclobutanedicarboxylate is as follows:The major product is tetraethy1 1,1,5,5-pentanetetra-carboxylate II with diethyl malonate. To eliminate this side reaction, II was independently prepared by the addition of hydrogen bromide to diethyl allylmalonate (I) and then cyclized to II by treatment with sodium ethylate. The over-all yield from I is about 50%.
| [Synthesis]
GENERAL METHOD: Diethyl malonate (2.53 mL, 17 mmol), 1,3-dibromopropane (22 mmol), potassium carbonate (K2CO3, 5.7 g, 42 mmol) and tetrabutylammonium bromide (TBAB, 0.27 g, 0.08 mmol) were added to dry N,N-dimethylformamide (DMF). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the solvent was removed by rotary evaporator and the residue was extracted three times with ethyl acetate (100 mL). The organic layers were combined, washed with water and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to give diethyl cyclobutyl-1,1-dicarboxylate as a colorless oil (89% yield). | [References]
[1] Molecules, 2016, vol. 21, # 5,
[2] Journal of Organic Chemistry, 1993, vol. 58, # 27, p. 7709 - 7717
[3] Journal of Fluorine Chemistry, 2000, vol. 102, # 1-2, p. 141 - 146
[4] Journal of Organic Chemistry, 1949, vol. 14, p. 1036
[5] Journal of the Chemical Society, 1887, vol. 51, p. 2 |
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