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| | Cyclohexane-1,3-dicarboxylic acid dimethyl ester Basic information | | Application |
| Product Name: | Cyclohexane-1,3-dicarboxylic acid dimethyl ester | | Synonyms: | Dimethyl 1,3-cyclohexane dicarboxylate;1,3-dimethyl cyclohexane-1,3-dicarboxylate;1,3-Cyclohexanedicarboxylic acid, 1,3-dimethyl ester;Dimethyl cyclohexane-1,3-dixarboxylate;diMethyl cyclohexane-1,3-dicarboxylate;Cyclohexane-1,3-dicarboxylic acid dimethyl ester | | CAS: | 62638-06-6 | | MF: | C10H16O4 | | MW: | 200.23 | | EINECS: | | | Product Categories: | | | Mol File: | 62638-06-6.mol |  |
| | Cyclohexane-1,3-dicarboxylic acid dimethyl ester Chemical Properties |
| Boiling point | 258.1±15.0℃ (760 Torr) | | density | 1.102±0.06 g/cm3 (20 ºC 760 Torr) | | refractive index | 1.4592 (589.3 nm 18℃) | | Fp | 120.7±18.8℃ | | storage temp. | Sealed in dry,Room Temperature | | Appearance | Colorless to light yellow Liquid |
| | Cyclohexane-1,3-dicarboxylic acid dimethyl ester Usage And Synthesis |
| Application | Dimethyl 1,3-cyclohexanoate can be used as a pharmaceutical synthesis intermediate and an organic synthesis intermediate, mainly in laboratory research and development processes and chemical and pharmaceutical synthesis processes. | | Synthesis | 1. cyclohexane-1,3-dicarboxylic acid (10.32 g, 60 mmol) was dissolved in methanol (130 mL).
2. Concentrated sulfuric acid (2.5 mL) was added as a catalyst and the reaction mixture was heated to reflux and stirred for 16 hours.
3. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove most of the methanol.
4. The residue was adjusted to pH 7 with saturated aqueous sodium bicarbonate.
5. The aqueous phase was extracted with ethyl acetate (200 mL × 3) and the organic layers were combined. 6.
6. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give dimethyl 1,3-cyclohexanedioate as a colorless oil (12 g, 100% yield). 7. The product was analyzed by 1H NMR.
7. The product was characterized by 1H NMR (400 MHz, DMSO-d6) and mass spectrometry (ESI): 1H NMR δ 3.61 (s, 6H), 2.69-1.13 (m, 10H); MS (ESI) m/e [M + 1] 201.1. | | References | [1] Patent: WO2016/161960, 2016, A1. Location in patent: Paragraph 0542
[2] Acta Crystallographica Section C: Crystal Structure Communications, 2013, vol. 69, # 7, p. 727 - 729
[3] Patent: WO2012/88365, 2012, A1. Location in patent: Page/Page column 24
[4] Patent: WO2013/40535, 2013, A2. Location in patent: Page/Page column 23
[5] Patent: WO2016/106623, 2016, A1. Location in patent: Page/Page column 122 |
| | Cyclohexane-1,3-dicarboxylic acid dimethyl ester Preparation Products And Raw materials |
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