Dimethyl cyclopentane-1,3-dicarboxylate

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
EINECS:
Product Categories:
Mol File:2435-36-1.mol
Dimethyl cyclopentane-1,3-dicarboxylate Structure
Dimethyl cyclopentane-1,3-dicarboxylate Chemical Properties
Boiling point 241℃
density 1.135
Fp 113℃
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Oil
color Clear Colourless
Safety Information
MSDS Information
Dimethyl cyclopentane-1,3-dicarboxylate Usage And Synthesis
UsesDimethyl 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.
SynthesisA 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.
Dimethyl cyclopentane-1,3-dicarboxylate Preparation Products And Raw materials
METHYL 1-CYCLOPENTENE-1-CARBOXYLATE POTASSIUM CYCLOPENTYLTRIFLUOROBORATE 1,3-CYCLOPENTANEDIOL Dimethyl cyclopentane-1,3-dicarboxylate BIS(1H,1H,7H-PERFLUOROHEPTYL)DICAMPHORATE DIBUTYLNORCAMPHORATE DIMETHYL (1R,3S)-1,2,2-TRIMETHYLCYCLOPENTANE-1,3-DICARBOXYLATE 1,2,3,4-CYCLOPENTANETETRACARBOXYLIC DIANHYDRIDE DIMETHYL CYCLOPENTANE-1,3-DICARBOXYLATE RARECHEM AQ C5 0005 DIMETHYL CAMPHORATE AKOS BBS-00001928 SALOR-INT L161314-1EA 1,2,3,4-CYCLOPENTANETETRACARBOXYLIC ACID

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.