methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate

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methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate Basic information
Product Name:methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate
Synonyms:methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate;1,4-Dioxaspiro[4.5]decane-8-carboxylic Acid Methyl Ester
CAS:26845-47-6
MF:C10H16O4
MW:200.23
EINECS:
Product Categories:Aliphatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:26845-47-6.mol
methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate Structure
methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate Chemical Properties
Boiling point 96-100 °C
density 1.15±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form clear liquid
color Colorless to Almost colorless
CAS DataBase Reference26845-47-6
Safety Information
HS Code 2932.99.9090
MSDS Information
methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate Usage And Synthesis
Usesmethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate is a reagnet used in the preparation of pharmaceutical compounds such as high affinity H3 receptor agonists and reverse hydroxamate-based selective TACE inhibitors.
Synthesis
Methyl 4-ketocyclohexanecarboxylate

6297-22-9

Ethylene glycol

107-21-1

methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate

26845-47-6

Step 1: Synthesis of methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate 1.3 g of methyl 4-oxocyclohexanecarboxylate, 0.64 g of ethylene glycol and 0.14 g of p-toluenesulfonic acid were added to 40 mL of toluene. The mixed solution was refluxed and stirred overnight in the presence of a Dean-Stark water separator to remove the water generated. Upon completion of the reaction, the toluene solvent was removed by distillation under reduced pressure. Subsequently, the reaction mixture was separated by extraction with 50 mL of diethyl ether and 50 mL of water. The organic phase was dried with anhydrous magnesium sulfate, filtered and purified by reduced pressure distillation (138~145 °C, 15 mmHg) to afford 0.42 g of the oily target product methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate. The product was characterized by NMR (300 MHz, CDCl3): δ 3.95 (s, 4H), 3.67 (s, 3H), 2.36~2.32 (m, 1H), 1.94~1.91 (m, 2H), 1.83~1.75 (m, 4H), 1.61~1.55 (m, 2H).

References[1] Journal of Organic Chemistry, 1997, vol. 62, # 16, p. 5284 - 5292
[2] Recueil: Journal of the Royal Netherlands Chemical Society, 1980, vol. 99, # 2, p. 53 - 57
[3] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 23, p. 6309 - 6323
[4] Patent: WO2007/6760, 2007, A1. Location in patent: Page/Page column 109-110; 130-131
[5] Patent: EP1860089, 2007, A1. Location in patent: Page/Page column 21-22
methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate Preparation Products And Raw materials
Raw materialsMethyl 4-ketocyclohexanecarboxylate-->Ethylene glycol-->p-Toluenesulfonic acid monohydrate-->Toluene
Tag:methyl 1,4-dioxaspiro[4.5]decane-8-carboxylate(26845-47-6) Related Product Information
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