alpha-ethoxy-p-cresol CAS 57726-26-8
alpha-ethoxy-p-cresol Basic information
| Product Name: | alpha-ethoxy-p-cresol |
| Synonyms: | alpha-ethoxy-p-cresol;Phenol, 4-(ethoxymethyl)-;4-(Ethoxymethyl)phenol;4-Ethoxymethylphenol;alpha-Ethoxy-p-creso;p-Hydroxybenzyl ethyl ether;4-hydroxybenzyl ethyl ether;p-Hydroxybenzyl Et ether |
| CAS: | 57726-26-8 |
| MF: | C9H12O2 |
| MW: | 152.19 |
| EINECS: | 260-918-4 |
| Product Categories: | |
| Mol File: | 57726-26-8.mol |
alpha-ethoxy-p-cresol Chemical Properties
| storage temp. | Inert atmosphere,Room Temperature |
| form | Solid |
| color | White to off-white |
| LogP | 1.699 (est) |
Safety Information
| Uses | 4-(Ethoxymethyl)phenol (p-Hydroxybenzyl Et ether) is a potent antioxidant from Amburana cearensis leaf extract, with in vitro cytogenotoxic properties. Amburana cearensis leaves can be used foe the research of respiratory diseases and inflammations[1]. |
| Definition | ChEBI: 4-(Ethoxymethyl)phenol is a benzyl ether. |
| Synthesis | 64-17-5 623-05-2 57726-26-8 General procedure for the synthesis of 4-(ethoxymethyl)phenol from ethanol and p-hydroxybenzyl alcohol: refer to the operation of Example 2, but substitute ethanol for methanol. After completion of the reaction, the residue was purified by reduced pressure distillation (boiling point: 110-119°C/1.5 Torr) to obtain 4-ethoxymethylphenol in 75% yield and 98% HPLC purity. The operation was as follows: in a 200 mL three-necked flask equipped with a thermometer, a three-way stopper and a stirrer, 15.0 g (0.12 mol) of p-hydroxybenzyl alcohol and 69 g of ethanol were added under nitrogen protection, followed by 0.06 g of nitromethane. A mixed solution consisting of 0.45 g of hydrochloric acid and 3.0 g of ethanol was slowly added dropwise under stirring at room temperature, and then the reaction mixture was stirred at 35 °C for 3 hours. At the end of the reaction, HPLC analysis showed an area percentage of 99%. Next, a mixed solution comprising 0.38 g of imidazole (manufactured by Aldrich Co., Ltd.) and 1.1 g of ethanol was added dropwise for neutralization, followed by concentration under reduced pressure to remove ethanol. To the concentrate, 60 g of isopropyl ether (produced by Nacalai Tesque, Inc.) and 22.5 g of water were added and the organic layer was further washed with 27 g of water and 0.26 g of acetic acid (produced by Nacalai Tesque). After washing the organic layer twice with water, the organic layer was concentrated, the crystal seed was added and slowly cooled to about 8°C. The precipitated crystals were filtered and dried to give 12.0 g (yield: 72%) of colorless 4-methoxymethylphenol with 99% HPLC purity. |
| References | [1] José Rafael da Silva Araujo, et al. Antioxidant and in vitro cytogenotoxic properties of Amburana cearensis (Allem?o) A.C.Sm. leaf extract. Drug Chem Toxicol. 2021 Dec 14;1-9. DOI:10.1080/01480545.2021.2011313 |
alpha-ethoxy-p-cresol Preparation Products And Raw materials
| Raw materials | Ethanol-->4-Hydroxybenzyl alcohol-->Water-->Hydrochloric acid |
