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Dimethyl cyclopentane-1,3-dicarboxylate

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Dimethyl cyclopentane-1,3-dicarboxylate Basic information

Product Name:
Dimethyl cyclopentane-1,3-dicarboxylate
Synonyms:
  • DIMETHYLNORCAMPHORATE
  • 1,3-Cyclopentanedicarboxylic acid dimethyl ester
  • Dimethyl=1,3-cyclopentanedicarboxylate
  • Cyclopentane-1,3-dicarboxylic acid dimethyl ester
  • Norcamphoric acid, dimethyl ester
  • 1,3-Bis(methoxycarbonyl)cyclopentane
  • 1,3-diMethyl cyclopentane-1,3-dicarboxylate
  • 1,3-Cyclopentanedicarboxylic acid, 1,3-diMethyl ester
CAS:
2435-36-1
MF:
C9H14O4
MW:
186.21
Mol File:
2435-36-1.mol
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Dimethyl cyclopentane-1,3-dicarboxylate Chemical Properties

Boiling point:
241℃
Density 
1.135
Flash point:
113℃
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Oil
color 
Clear Colourless
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Dimethyl cyclopentane-1,3-dicarboxylate Usage And Synthesis

Uses

Dimethyl cyclopentane-1,3-dicarboxylate (cas# 2435-36-1) is a useful research chemical, It can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis

A 5-L, 3-neck, roundbottom flask was equipped with a mechanical stirrer, a J-KEM temperature controller, and a reflux condenser. The flask was charged with cyclopentane-l,3-dicarboxylic acid(357 g, 2.262 mol) and methanol (1.75 L). The solution was cooled to 7 °C using anice/water bath. Concentrated sulfuric acid (70 mL) was added dropwise over 30 minresulting in an exotherm up to 12 °C. The reaction mixture was heated to reflux andstirred for 16 h when TLC analysis (10 percent methanol/ethyl acetate) indicated that thereaction was complete. The reaction mixture was concentrated, redissolved in methyl- 179 -ATI-2514175vl tert-butyl ether, and washed with saturated aqueous sodium bicarbonate (2 x 150 mL) and brine (2 x 150 mL). The organic layer was dried over sodium sulfate, filtered, and concentrated. The resulting clear oil was dissolved in hexane (2 L) and treated with a 2 N aqueous sodium hydroxide solution (950 mL) until the pH ~ 10. The layers were separated and the aqueous layer was extracted with hexane (4 x 1 L). The organic layers were combined, dried over sodium sulfate, filtered, and concentrated to provide 360 g (100percent) of dimethyl cyclopentane-l,3-dicarboxylate as a clear oil.

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