diethyl 1,1-cyclopentanedicarboxylate

diethyl 1,1-cyclopentanedicarboxylate Suppliers list
Company Name: Creasyn Finechem(Tianjin) Co., Ltd.  
Tel: 022-83946278 13820372920
Email: sales@creasyn.com
Company Name: Shanghai Yuanding Chem. Sci. & Tech. Co., Ltd.  
Tel: 21-57721279 18121011378
Email: sales@shydchem.com.cn
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: 021-58170097
Email: info@topbiochem.com
Company Name: ShangHai ZiCheng Med-Pharm Technology Company Ltd.  
Tel: 021-56710790 18721468858
Email: wangyh@fudan.edu.cn
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com

diethyl 1,1-cyclopentanedicarboxylate manufacturers

diethyl 1,1-cyclopentanedicarboxylate Basic information
Product Name:diethyl 1,1-cyclopentanedicarboxylate
Synonyms:diethyl 1,1-cyclopentanedicarboxylate;1,1-Cyclopentanedicarboxylic acid, diethyl ester;Cyclopentane-4,4-dicarboxylic acid diethyl ester;Ai3-11605;Einecs 224-024-8;1,1-Bis(ethoxycarbonyl)cyclopentane;1,1-Cyclopentanedicarboxylic acid 1,1-diethyl ester;NSC 67352
CAS:4167-77-5
MF:C11H18O4
MW:214.26
EINECS:224-024-8
Product Categories:
Mol File:4167-77-5.mol
diethyl 1,1-cyclopentanedicarboxylate Structure
diethyl 1,1-cyclopentanedicarboxylate Chemical Properties
Boiling point 246℃
density 1.096
refractive index 1.4450
Fp 110℃
storage temp. Sealed in dry,Room Temperature
form solid
AppearanceColorless to light yellow Liquid
InChI1S/C11H18O4/c1-3-14-9(12)11(7-5-6-8-11)10(13)15-4-2/h3-8H2,1-2H3
InChIKeyNAKRHRXBVSLQAO-UHFFFAOYSA-N
SMILESO=C(C1(C(OCC)=O)CCCC1)OCC
Safety Information
WGK Germany WGK 3
HS Code 29172090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
diethyl 1,1-cyclopentanedicarboxylate Usage And Synthesis
Synthesis
1,4-Dibromobutane

110-52-1

Diethyl malonate

105-53-3

diethyl 1,1-cyclopentanedicarboxylate

4167-77-5

1. 1,4-dibromobutane and diethyl malonate are dissolved in DMF under nitrogen protection. 2. Potassium carbonate (K2CO3) and tetrabutylammonium fluoride (TBAF) were added sequentially to the above solution. 3. The reaction mixture was stirred at room temperature overnight. 4. 4. Upon completion of the reaction, the reaction was quenched with 200 mL of cold water. 5. The reaction mixture was extracted with a 10% ethyl acetate/hexane solvent mixture (3 x 150 mL). 6. The organic layers were combined and washed sequentially with half-saturated brine (150 mL x 2) and brine (150 mL). 7. The organic layer was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated to dryness. 8. The residue was purified by fast silica gel column chromatography using 2% ethyl acetate/hexane as eluent to give 36.7 g (84% yield) of ethyl 1,1-dicarboxylate cyclopentane as a colorless oil.

References[1] Tetrahedron Letters, 2005, vol. 46, # 4, p. 635 - 638
[2] Patent: WO2013/185202, 2013, A1. Location in patent: Paragraph 00280; 00281
[3] Patent: WO2015/95227, 2015, A2. Location in patent: Page/Page column 96; 97
[4] Journal of Medicinal Chemistry, 2018, vol. 61, # 3, p. 989 - 1000
[5] Journal of the American Chemical Society, 2010, vol. 132, # 41, p. 14409 - 14411
diethyl 1,1-cyclopentanedicarboxylate Preparation Products And Raw materials
Raw materials1,4-Dibromobutane-->Diethyl malonate-->Tetrabutylammonium Fluoride-->N,N-Dimethylformamide-->Potassium carbonate
Preparation ProductsCyclopentane-1,1-diacetic acid
Tag:diethyl 1,1-cyclopentanedicarboxylate(4167-77-5) Related Product Information
Phthalates Cyclopentane-1,1-dicarboxylic acid DIETHYLMALONIC ACID AKOS 315 CYCLOPENTANE-1,1-DIYLDIMETHANOL Butylmalonic acid diethyl 1,1-cyclopentanedicarboxylate DIETHYL 3-(BENZYLOXY)CYCLOPENTANE-1,1-DICARBOXYLATE