2-Hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride CAS 103577-66-8
2-Hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride Basic information
| Product Name: | 2-Hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride |
| Synonyms: | 2-trifluoro-ethoxy)-pyridin-2-yl]-Methanol;Lansoprazole hydroxy coMpound;3-Methyl-4-(2,2,2-Trifluoroethoxy)-2-Pyridinemethanol;2-hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethyoxy)pyridine hydrochloride;3-METHYL-4-(2,2,2-TRIFLUOROETHOXY)-2-PY&;2-PyridineMethanol,3-Methyl-4-(2,2,2-trifluoroethoxy)-;2-HYDROXYMETHYL-3-METHYL-4-(2,2,2-THIFLUOROETHOXY)PYRIDINE;2-HYDROXYMETHYL-3-METHYL-4-(2,2,2-TRIFLUOROETHOXY) PYRIDINE |
| CAS: | 103577-66-8 |
| MF: | C9H10F3NO2 |
| MW: | 221.18 |
| EINECS: | 1308068-626-2 |
| Product Categories: | |
| Mol File: | 103577-66-8.mol |
2-Hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride Chemical Properties
| Melting point | 93-94 °C(Solv: isopropyl ether (108-20-3); hexane (110-54-3)) |
| Boiling point | 273.6±40.0 °C(Predicted) |
| density | 1.303±0.06 g/cm3(Predicted) |
| storage temp. | Sealed in dry,Room Temperature |
| solubility | DMSO (Slightly), Methanol (Slightly) |
| pka | 13.17±0.10(Predicted) |
| form | Solid |
| color | Pale Beige to Light Brown |
| Stability: | Light Sensitive |
| CAS DataBase Reference | 103577-66-8(CAS DataBase Reference) |
Safety Information
| Chemical Properties | Brown Solid |
| Uses | Intermediate in the preparation of Lansoprazole (L175000) impurity. |
| Synthesis | 112525-75-4 103577-66-8 e) 34.8 g of 2-acetoxymethyl-3-methyl-4-(trifluoroethoxy)pyridine (equivalent to 18.7 g, 0.071 mol) obtained in the previous step was used as raw material, which was dissolved in 15 ml of a solvent mixture of methanol/water (1:1) at room temperature. The pH of the reaction system was adjusted with 33% aqueous sodium hydroxide solution to 13. The reaction was carried out at a temperature of 25 to 30 °C and a pH range of 12.5 to 13.5 and the progress of the reaction was monitored by HPLC. Upon completion of the reaction, the reaction mixture was neutralized with 36% hydrochloric acid and subsequently extracted with dichloromethane. The organic layer was dried and concentrated to 60 ml. The yield of the product 2-hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine was 95-97% as determined by HPLC. |
| References | [1] Journal of Medicinal Chemistry, 1992, vol. 35, # 3, p. 438 - 450 [2] Patent: EP1681056, 2006, A1. Location in patent: Page/Page column 8 |
2-Hydroxymethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride Preparation Products And Raw materials
| Raw materials | 2-Acetoxymethyl1-3-Methyl-4- |
| Preparation Products | 2-[3-Methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methylthio-1H-benzimidazole |
